Canonical Allele Identifier: PA287288
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127571
ClinVar RCV Id: RCV000115391 RCV000412014 RCV000477204 RCV000588221 RCV003467040
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala81Val
CA010271
NM_000179.3:c.242C>T