Canonical Allele Identifier: PA2826627351
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1317113
ClinVar RCV Id: RCV001758985
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu689Asp
CA346754082
NM_001281492.2:c.2067G>C
CA346754083
NM_001281492.2:c.2067G>T