Canonical Allele Identifier: PA2826629038
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 231365
ClinVar RCV Id: RCV000216678 RCV000708893 RCV000704640 RCV001358640 RCV003469028
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu1151Gln
CA10578163
NM_001281492.2:c.3451G>C