Allele Registry

Canonical Allele Identifier: PA645453228

Gene: TMEM67 HGNC NCBI

ClinVar RCV:

RCV000262960

RCV000318190

RCV000372722

ClinVar Variation:

363922

HGVS (amino-acid)	Matching Registered Transcripts
NP_714915.3:p.Tyr567Ser	CA10631755 NM_153704.6:c.1700A>C