Canonical Allele Identifier: PA2825088590
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1778619
ClinVar RCV Id: RCV002398956

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gln572Arg
CA346748606
NM_000179.3:c.1715A>G