Canonical Allele Identifier: PA2826634269
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 188357
ClinVar RCV Id: RCV000168389 RCV000220509 RCV000656996 RCV003995626 RCV003316071
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr17Met
CA016673
NM_001281494.2:c.50C>T