Canonical Allele Identifier: PA2826625395
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 419950
ClinVar RCV Id: RCV000563224 RCV000629709 RCV001704606 RCV004003316
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser230Gly
CA067126
NM_001281492.2:c.688A>G