Canonical Allele Identifier: PA106880
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 13350
ClinVar RCV Id: RCV000014278 RCV000158002 RCV000520164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Phe53Ser
CA279966
NM_002755.4:c.158T>C