Canonical Allele Identifier: PA2826628787
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val1102del
CA013845
NM_001281492.2:c.3304_3306del