Canonical Allele Identifier: PA2580263450
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2004312
ClinVar RCV Id: RCV002816013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Asn122Ser
CA7623913
NM_002755.4:c.365A>G