Canonical Allele Identifier: PA2741991797
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2716942
ClinVar RCV Id: RCV003539695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.His243Asp
CA304449328
NM_030662.4:c.727C>G