Canonical Allele Identifier: PA2826636973
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233859
ClinVar RCV Id: RCV000219717 RCV000792117 RCV003463593 RCV003998583
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu690Gly
CA10578124
NM_001281494.2:c.2069A>G