Canonical Allele Identifier: PA296144
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 40828
ClinVar RCV Id: RCV000158029 RCV000680294 RCV001261064 RCV001480813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Asp285Asn
CA296142
NM_030662.4:c.853G>A