Allele Registry

Canonical Allele Identifier: PA2826587197

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000491517

RCV000759147

RCV000797850

RCV003316642

RCV003464057

RCV004003460

ClinVar Variation:

428382

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Phe1021Ser	CA46719891 NM_001281494.2:c.3062T>C