Canonical Allele Identifier: PA915964999
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 801698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.His766Gln
CA068773
NM_000179.3:c.2298T>G
CA346753012
NM_000179.3:c.2298T>A