Canonical Allele Identifier: PA645474749
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230023
ClinVar RCV Id: RCV000223424 RCV000765670 RCV003997795 RCV000477055 RCV001550360 RCV004532776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala609Ser
CA031583
NM_000251.3:c.1825G>T