Canonical Allele Identifier: PA2825089458
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1789397
ClinVar RCV Id: RCV002446413

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly770Val
CA346753117
NM_000179.3:c.2309G>T