Allele Registry

Canonical Allele Identifier: PA2826630293

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001349078

ClinVar Variation:

1044775

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Glu191Ala	CA346746013 NM_001281493.2:c.572A>C