Canonical Allele Identifier: PA2826628587
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 485876
ClinVar RCV Id: RCV000571078
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu1057_Ser1058del
CA658655722
NM_001281492.2:c.3169_3174del