Allele Registry

Canonical Allele Identifier: PA2826634693

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001753358

RCV001868750

ClinVar Variation:

1318811

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Phe159Ser	CA346745004 NM_001281494.2:c.476T>C