Canonical Allele Identifier: PA2826637285
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237180
ClinVar Variation Id: 1728704
ClinVar RCV Id: RCV002322894

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asn763Lys
CA070349
NM_001281494.2:c.2289C>G
CA346757855
NM_001281494.2:c.2289C>A