Canonical Allele Identifier: PA2826625435
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127554
ClinVar RCV Id: RCV000115368 RCV000210148 RCV000212645 RCV000415687 RCV000528613 RCV000662663 RCV001193101
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr239Ile
CA008045
NM_001281492.2:c.716C>T