Canonical Allele Identifier: PA2825091808
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1732697
ClinVar RCV Id: RCV002454930
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.[Glu1187_Thr1189delinsVal;Phe1191del]
CA2580067225
NM_000179.3:c.3560_3568del