Canonical Allele Identifier: PA2826627768
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 619580
ClinVar RCV Id: RCV000758672 RCV002440585 RCV002533820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala785Thr
CA346755400
NM_001281492.2:c.2353G>A