Allele Registry

Canonical Allele Identifier: PA116919

Gene: PANK2 HGNC NCBI

ClinVar RCV:

RCV003985014

ClinVar Variation:

4553

HGVS (amino-acid)	Matching Registered Transcripts
NP_079236.3:p.Ser60Pro	CA116918 NM_024960.6:c.178T>C