Allele Registry

Canonical Allele Identifier: PA645385035

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000491517

RCV000759147

RCV000797850

RCV003316642

RCV003464057

RCV004003460

ClinVar Variation:

428382

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Phe1323Ser	CA46719891 NM_000179.3:c.3968T>C