Allele Registry

Canonical Allele Identifier: PA916011846

Gene: MSH6 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000160665

RCV000206352

RCV000565934

RCV000656894

RCV000662428

RCV000708864

RCV001030492

RCV002484997

ClinVar Variation:

182620

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Tyr95Cys	CA008291 NM_001281494.2:c.284A>G