Canonical Allele Identifier: PA299345
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182573
ClinVar RCV Id: RCV000160604 RCV001308489
ClinVar Variation Id: 1787461
ClinVar RCV Id: RCV002425580
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr732Ser
CA020205
NM_000251.3:c.2195C>G
CA346729412
NM_000251.3:c.2194A>T