Canonical Allele Identifier: PA2826633918
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2720332
ClinVar RCV Id: RCV003595292
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro1007_Glu1008insAspAsnLeuPro
CA2697548082
NM_001281493.2:c.3012_3023dup