Allele Registry

Canonical Allele Identifier: PA2826631921

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000470821

RCV000491946

RCV000759137

RCV004001855

ClinVar Variation:

410521

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Ile570Val	CA16611154 NM_001281493.2:c.1708A>G