Canonical Allele Identifier: PA2826629643
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 919753
ClinVar RCV Id: RCV001178071
ClinVar Variation Id: 3230488
ClinVar RCV Id: RCV004520639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu35Phe
CA346741258
NM_001281493.2:c.105G>C
CA346741261
NM_001281493.2:c.105G>T