Allele Registry

Canonical Allele Identifier: PA658681197

Gene: MSH6 HGNC NCBI

ClinVar Variation Id: 487033

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Thr1010Ile	CA069975 NM_000179.3:c.3029C>T