Canonical Allele Identifier: PA2826636107
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1063318

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asn487del
CA2499216115
NM_001281494.2:c.1459_1461del