Canonical Allele Identifier: PA185380
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 179898
ClinVar RCV Id: RCV000156699 RCV000700016
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Val211Ile
CA185378
NM_002755.4:c.631G>A