Canonical Allele Identifier: PA330399
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89239
ClinVar Variation Id: 1784644
ClinVar RCV Id: RCV002419673

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu675Asp
CA009565
NM_000179.3:c.2025G>C
CA346750709
NM_000179.3:c.2025G>T