Canonical Allele Identifier: PA2826627524
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 489985
ClinVar RCV Id: RCV000579759 RCV001371208
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser730Cys
CA346754780
NM_001281492.2:c.2189C>G