Canonical Allele Identifier: PA645423276
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 375984
ClinVar RCV Id: RCV000441191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Asn382His
CA16602459
NM_002755.4:c.1144A>C