Canonical Allele Identifier: PA2825089435
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2756264
ClinVar RCV Id: RCV003593804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Cys765Tyr
CA346752974
NM_000179.3:c.2294G>A