Allele Registry

Canonical Allele Identifier: PA277792

Gene: TMEM67 HGNC NCBI

ClinVar RCV:

RCV000198666

RCV000201726

RCV000624166

RCV001090385

RCV001814102

RCV002283466

ClinVar Variation:

216826

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135773.1:p.Asn161Ser	CA277789 NM_001142301.1:c.482A>G