Allele Registry

Canonical Allele Identifier: PA2826020677

Gene: PALLD HGNC NCBI

ClinVar RCV:

RCV002629397

ClinVar Variation:

2198451

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159582.1:p.Asp335Gly	CA3135900 NM_001166110.2:c.1004A>G