Canonical Allele Identifier: PA2499291937
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1027629
ClinVar RCV Id: RCV001328431 RCV002546258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Ala399Thr
CA403380630
NM_030662.4:c.1195G>A