Allele Registry

Canonical Allele Identifier: PA115613

Gene: PALLD HGNC NCBI

ClinVar RCV:

RCV000002681

RCV000160876

RCV000168440

RCV003894786

ClinVar Variation:

2572

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159582.1:p.Pro139Ser	CA115612 NM_001166110.2:c.415C>T