Canonical Allele Identifier: PA2826625968
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2071259
ClinVar RCV Id: RCV002975438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Met369Ile
CA346746167
NM_001281492.2:c.1107G>A
CA346746168
NM_001281492.2:c.1107G>C
CA346746174
NM_001281492.2:c.1107G>T