Canonical Allele Identifier: PA2573291658
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1525536
ClinVar RCV Id: RCV002036760 RCV003481257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Gly381Ser
CA9090690
NM_030662.4:c.1141G>A