Canonical Allele Identifier: PA2573291479
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1447640
ClinVar RCV Id: RCV001979923 RCV004043833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Ile130Val
CA403391454
NM_030662.4:c.388A>G