Canonical Allele Identifier: PA2825087334
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 842691
ClinVar RCV Id: RCV001045149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asn307Asp
CA346740736
NM_000179.3:c.919A>G