Canonical Allele Identifier: PA296153
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 180907
ClinVar RCV Id: RCV000158032 RCV001850203 RCV003325190
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Tyr324Cys
CA296151
NM_030662.4:c.971A>G