Canonical Allele Identifier: PA2826626753
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2822760
ClinVar RCV Id: RCV003761037
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser547Gly
CA346750718
NM_001281492.2:c.1639A>G