Allele Registry

Canonical Allele Identifier: PA170044

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000132542

RCV002228511

RCV003998152

ClinVar Variation:

143023

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Tyr730Cys	CA009841 NM_000179.3:c.2189A>G