Canonical Allele Identifier: PA2826631051
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89236
ClinVar RCV Id: RCV001357734 RCV003593868
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser364Pro
CA009527
NM_001281493.2:c.1090T>C