Canonical Allele Identifier: PA2826627230
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1063318

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asn659del
CA2499216115
NM_001281492.2:c.1975_1977del