Allele Registry

Canonical Allele Identifier: PA2741899941

Gene: TPD52L1 HGNC NCBI

ClinVar RCV:

RCV004350942

ClinVar Variation:

2606908

HGVS (amino-acid)	Matching Registered Transcripts
NP_003278.1:p.Met30Thr	CA147112656 NM_003287.4:c.89T>C