Canonical Allele Identifier: PA296159
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 40842
ClinVar RCV Id: RCV000158034 RCV000546588 RCV000781515
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Arg371Gln
CA296157
NM_030662.4:c.1112G>A