ClinGen Allele Registry
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Canonical Allele Identifier:
PA116920
Gene: PANK2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV003985014
ClinVar Variation:
4553
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_705904.1:p.Ser60Pro
CA116918
NM_153640.4:c.178T>C