Allele Registry

Canonical Allele Identifier: PA330514

Gene: MSH6 HGNC NCBI

ClinVar Allele:

94852

ClinVar RCV:

RCV000524174

RCV000573399

RCV001800369

RCV003460682

RCV003997088

ClinVar Variation:

89378

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Tyr1128Cys	CA012724 NM_000179.3:c.3383A>G