Canonical Allele Identifier: PA658680701
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg577Ser
CA346748747
NM_000179.3:c.1729C>A