Canonical Allele Identifier: PA2580263507
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2319773
ClinVar RCV Id: RCV004164178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Asn382Lys
CA392939103
NM_002755.4:c.1146C>A
CA392939104
NM_002755.4:c.1146C>G