Allele Registry

Canonical Allele Identifier: PA2580152511

Gene: PALLD HGNC NCBI

ClinVar RCV:

RCV002629397

ClinVar Variation:

2198451

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159580.1:p.Asp839Gly	CA3135900 NM_001166108.2:c.2516A>G