Canonical Allele Identifier: PA2829112104
Gene: PANK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1358893
ClinVar RCV Id: RCV001894352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373322.1:p.Trp356Cys
CA9750825
NM_001386393.1:c.1068G>C
CA311035741
NM_001386393.1:c.1068G>T