Canonical Allele Identifier: PA2826635584
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455171
ClinVar RCV Id: RCV000528067 RCV000580603 RCV001192423 RCV003153675
ClinVar Variation Id: 838100
ClinVar RCV Id: RCV001039583 RCV002416339
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp365Glu
CA346750666
NM_001281494.2:c.1095T>G
CA346750667
NM_001281494.2:c.1095T>A