Canonical Allele Identifier: PA2826637338
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1692256
ClinVar RCV Id: RCV002257122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Pro775Ala
CA346758037
NM_001281494.2:c.2323C>G