Allele Registry

Canonical Allele Identifier: PA357754

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000206769

RCV000216982

RCV003997670

ClinVar Variation:

221144

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu220Gly	CA073311 NM_000179.3:c.659A>G