Canonical Allele Identifier: PA356997
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 223140
ClinVar RCV Id: RCV000208748 RCV000428485 RCV000421288 RCV000438528 RCV002051691 RCV002254287
ClinVar Variation Id: 376174
ClinVar RCV Id: RCV000419591 RCV000420720 RCV000427279 RCV000429649 RCV000430292 RCV000436816 RCV000437917
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Lys57Asn
CA356995
NM_002755.4:c.171G>T
CA16602629
NM_002755.4:c.171G>C