Allele Registry

Canonical Allele Identifier: PA658744488

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000583660

RCV000806695

RCV002466543

ClinVar Variation:

491994

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Pro293Ser	CA073534 NM_000179.3:c.877C>T