Allele Registry

Canonical Allele Identifier: PA119069

Gene: PEX12 HGNC NCBI

ClinVar RCV:

RCV000008220

ClinVar Variation:

7778

HGVS (amino-acid)	Matching Registered Transcripts
NP_000277.1:p.Arg91Ser	CA119068 NM_000286.3:c.273A>T CA399138486 NM_000286.3:c.273A>C