Canonical Allele Identifier: PA116917
Gene: PANK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4548
ClinVar RCV Id: RCV000004807 RCV000132732 RCV000190815 RCV000224470 RCV001588799 RCV002496261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_705904.1:p.Gly230Arg
CA116915
NM_153640.4:c.688G>A
CA408120327
NM_153640.4:c.688G>C