Canonical Allele Identifier: PA2826624867
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455341
ClinVar RCV Id: RCV000526816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly107Arg
CA346739987
NM_001281492.2:c.319G>A
CA346739988
NM_001281492.2:c.319G>C