Canonical Allele Identifier: PA2826635614
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 422162
ClinVar RCV Id: RCV000480051
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly372Val
CA16617664
NM_001281494.2:c.1115G>T