Canonical Allele Identifier: PA2826627636
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 619578
ClinVar RCV Id: RCV000758670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu757Pro
CA346755201
NM_001281492.2:c.2270T>C