Canonical Allele Identifier: PA2499229408
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1008737
ClinVar RCV Id: RCV001306118 RCV002437041
ClinVar Variation Id: 2866960
ClinVar RCV Id: RCV003759401
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Phe902Leu
CA346755323
NM_000179.3:c.2704T>C
CA346755329
NM_000179.3:c.2706T>A
CA346755330
NM_000179.3:c.2706T>G