Canonical Allele Identifier: PA180892
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 177868
ClinVar RCV Id: RCV000154507 RCV000208747 RCV000412815 RCV000844676 RCV003453160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Tyr134Cys
CA180890
NM_030662.4:c.401A>G