Canonical Allele Identifier: PA2741991882
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2697388
ClinVar RCV Id: RCV003539526
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Val377Ala
CA403381042
NM_030662.4:c.1130T>C