Canonical Allele Identifier: PA2573096280
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1334256
ClinVar RCV Id: RCV001813671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Ile369Thr
CA403381182
NM_030662.4:c.1106T>C