Canonical Allele Identifier: PA645423255
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 376198
ClinVar RCV Id: RCV000422017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Val211Asp
CA16602653
NM_002755.4:c.632T>A