Canonical Allele Identifier: PA2573291630
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1416918
ClinVar RCV Id: RCV001935956 RCV004043549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Asp341Ala
CA403383321
NM_030662.4:c.1022A>C