Canonical Allele Identifier: PA2825092660
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_000170.1:p.Pro1309_Glu1310insAspAsnLeuPro
CA2697548082
NM_000179.3:c.3918_3929dup