Canonical Allele Identifier: PA2826637432
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89368
ClinVar RCV Id: RCV000164048 RCV000433110 RCV000412287 RCV000524168 RCV000985842 RCV003997087
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Arg793His
CA012443
NM_001281494.2:c.2378G>A