Canonical Allele Identifier: PA296184
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 180914
ClinVar RCV Id: RCV000158047 RCV002247552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Gly263Arg
CA296182
NM_030662.4:c.787G>A
CA403386550
NM_030662.4:c.787G>C