Allele Registry

Canonical Allele Identifier: PA160899

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000034494

RCV000074692

RCV000121577

RCV000128867

RCV000662448

RCV001082588

RCV004534719

ClinVar Variation:

41590

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Pro623Ala	CA009344 NM_000179.3:c.1867C>G