Canonical Allele Identifier: PA2826626875
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428334
ClinVar RCV Id: RCV000491970 RCV003493602
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Phe576Cys
CA346750971
NM_001281492.2:c.1727T>G