Allele Registry

Canonical Allele Identifier: PA277747

Gene: TMEM67 HGNC NCBI

ClinVar Allele:

214270

ClinVar RCV:

RCV000201641

RCV003330578

ClinVar Variation:

217715

HGVS (amino-acid)	Matching Registered Transcripts
NP_714915.3:p.Pro82Ser	CA277745 NM_153704.6:c.244C>T