Canonical Allele Identifier: PA2826634617
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 818925
ClinVar RCV Id: RCV001011016

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile140del
CA915943809
NM_001281494.2:c.418_420del