Canonical Allele Identifier: PA658826651
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 548921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala37del
CA658823250
NM_000179.3:c.105_107del