Allele Registry

Canonical Allele Identifier: PA2826857527

Gene: TPD52L1 HGNC NCBI

ClinVar RCV:

RCV004350942

ClinVar Variation:

2606908

HGVS (amino-acid)	Matching Registered Transcripts
NP_001287923.1:p.Met30Thr	CA147112656 NM_001300994.3:c.89T>C