Canonical Allele Identifier: PA2826625103
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479949
ClinVar RCV Id: RCV000561282 RCV003767109
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser162Thr
CA346740653
NM_001281492.2:c.485G>C