Allele Registry

Canonical Allele Identifier: PA2826634033

Gene: MSH6 HGNC NCBI

ClinVar Allele:

231587

ClinVar RCV:

RCV000216522

RCV000567812

RCV000630217

RCV001201279

RCV003463610

RCV003998616

ClinVar Variation:

234450

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Asn1025His	CA072425 NM_001281493.2:c.3073A>C