Canonical Allele Identifier: PA180872
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 40832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Pro298Leu
CA180870
NM_030662.4:c.893C>T