Canonical Allele Identifier: PA645425863
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 40772
ClinVar RCV Id: RCV000413006 RCV001063339 RCV000824945 RCV003153319 RCV003162290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Arg92Gly
CA9091063
NM_030662.4:c.274A>G