Canonical Allele Identifier: PA2580263478
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1761697
ClinVar RCV Id: RCV002412403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Asp267Glu
CA7624019
NM_002755.4:c.801T>A
CA392937232
NM_002755.4:c.801T>G