Canonical Allele Identifier: PA2826626582
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455163

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu508Val
CA346750196
NM_001281492.2:c.1522C>G
CA658655795
NM_001281492.2:c.1521_1522delinsTG