Allele Registry

Canonical Allele Identifier: PA2573306460

Gene: TMEM67 HGNC NCBI

ClinVar Variation Id: 1356294

HGVS (amino-acid)	Matching Registered Transcripts
NP_714915.3:p.Met252Ile	CA371687777 NM_153704.6:c.756G>T CA371687778 NM_153704.6:c.756G>C CA371687779 NM_153704.6:c.756G>A