Canonical Allele Identifier: PA2826628445
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89393
ClinVar RCV Id: RCV000131534 RCV000202300 RCV002513797 RCV002510780 RCV003450969 RCV004555853
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly1027Ser
CA012971
NM_001281492.2:c.3079G>A