Canonical Allele Identifier: PA658802284
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys885Asn
CA346755177
NM_000179.3:c.2655A>C
CA346755178
NM_000179.3:c.2655A>T