Allele Registry

Canonical Allele Identifier: PA2580153015

Gene: PALLD HGNC NCBI

ClinVar RCV:

RCV002952444

ClinVar Variation:

2058752

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159582.1:p.Ala101Thr	CA358796127 NM_001166110.2:c.301G>A