Allele Registry

Canonical Allele Identifier: PA2826633773

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000218648

RCV000462482

RCV000487307

RCV000589207

RCV003462524

ClinVar Variation:

233369

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Thr980Asn	CA10578165 NM_001281493.2:c.2939C>A