Canonical Allele Identifier: PA2829112076
Gene: PANK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 191359
ClinVar RCV Id: RCV000201489
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373322.1:p.Phe321Ser
CA279308
NM_001386393.1:c.962T>C