Canonical Allele Identifier: PA2826626308
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89218
ClinVar RCV Id: RCV000115381 RCV000524118 RCV000409690 RCV000491847 RCV003235029 RCV003997068 RCV003466935 RCV003993789
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg447Cys
CA009088
NM_001281492.2:c.1339C>T