Canonical Allele Identifier: PA2825087165
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2587335
ClinVar RCV Id: RCV003360813

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly289Ser
CA346740611
NM_000179.3:c.865G>A