Canonical Allele Identifier: PA2826625873
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2567483
ClinVar RCV Id: RCV003278526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gln345Pro
CA346745420
NM_001281492.2:c.1034A>C