Canonical Allele Identifier: PA2826636577
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2453198
ClinVar RCV Id: RCV003182653
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu597Asp
CA346755312
NM_001281494.2:c.1791A>C
CA346755313
NM_001281494.2:c.1791A>T