Canonical Allele Identifier: PA2826635282
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2693765
ClinVar RCV Id: RCV003594731 RCV004364920
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly297Glu
CA346749319
NM_001281494.2:c.890G>A