Canonical Allele Identifier: PA2826465046
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 489929
ClinVar RCV Id: RCV000579590 RCV001240812 RCV001574074 RCV004001257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Thr611Ala
CA346729112
NM_001258281.1:c.1831A>G