Allele Registry

Canonical Allele Identifier: PA163502

Gene: MSH6 HGNC NCBI

ClinVar Allele:

94660

ClinVar RCV:

RCV000128873

RCV000214282

RCV000791437

RCV002288560

RCV003460660

ClinVar Variation:

89186

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Leu435Pro	CA008468 NM_000179.3:c.1304T>C