Allele Registry

Canonical Allele Identifier: PA2826634575

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000162486

RCV000479506

RCV000500646

RCV000553513

RCV000582500

RCV003454393

RCV003995199

RCV004525833

ClinVar Variation:

183760

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Phe130Ser	CA008453 NM_001281494.2:c.389T>C