Allele Registry

Canonical Allele Identifier: PA2829847763

Gene: PALLD HGNC NCBI

ClinVar RCV:

RCV002629397

ClinVar Variation:

2198451

HGVS (amino-acid)	Matching Registered Transcripts
NP_057165.3:p.Asp822Gly	CA3135900 NM_016081.4:c.2465A>G