Canonical Allele Identifier: PA645423150
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 375978
ClinVar RCV Id: RCV000418731 RCV000429601 RCV002051704 RCV002254296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Gln56Pro
CA16602453
NM_002755.4:c.167A>C