Allele Registry

Canonical Allele Identifier: PA915989334

Gene: PALLD HGNC NCBI

ClinVar RCV:

RCV000707309

RCV004026750

ClinVar Variation:

583071

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159580.1:p.Asp995His	CA3136003 NM_001166108.2:c.2983G>C