Canonical Allele Identifier: PA2826463071
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_001245210.1:p.Gly137Arg
CA021564
NM_001258281.1:c.409G>A
CA346731082
NM_001258281.1:c.409G>C