Canonical Allele Identifier: PA2825089376
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1788278
ClinVar RCV Id: RCV002420181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu747Pro
CA346752593
NM_000179.3:c.2240T>C