Canonical Allele Identifier: PA2826587597
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 220947

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val1043_Ala1045del
CA348238
NM_001281494.2:c.3128_3136del