Allele Registry

Canonical Allele Identifier: PA658681357

Gene: MSH6 HGNC NCBI

ClinVar Allele:

451664

ClinVar RCV:

RCV000543217

RCV000572853

RCV000588973

RCV003470704

RCV004003694

ClinVar Variation:

455266

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Pro1169Ala	CA46717040 NM_000179.3:c.3505C>G