Canonical Allele Identifier: PA645423263
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 375983
ClinVar RCV Id: RCV000430494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Pro264Ser
CA16602458
NM_002755.4:c.790C>T