Allele Registry

Canonical Allele Identifier: PA2828242652

Gene: PALLD HGNC NCBI

ClinVar RCV:

RCV002629397

ClinVar Variation:

2198451

HGVS (amino-acid)	Matching Registered Transcripts
NP_001354499.1:p.Asp132Gly	CA3135900 NM_001367570.1:c.395A>G