Canonical Allele Identifier: PA287460
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127647
ClinVar RCV Id: RCV000115536 RCV000221014 RCV000409174 RCV000472250 RCV003997280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly203Arg
CA021564
NM_000251.3:c.607G>A
CA346731082
NM_000251.3:c.607G>C