Canonical Allele Identifier: PA357494
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 220488
ClinVar RCV Id: RCV000204953 RCV000565136 RCV000662576 RCV001558974 RCV003997640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu842Val
CA349143
NM_000251.3:c.2525A>T