Canonical Allele Identifier: PA2829112087
Gene: PANK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2627790
ClinVar RCV Id: RCV003389134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373322.1:p.Asp337Tyr
CA408117659
NM_001386393.1:c.1009G>T