Canonical Allele Identifier: PA2826625149
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 652505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Met173Leu
CA46706955
NM_001281492.2:c.517A>T
CA346740711
NM_001281492.2:c.517A>C