Canonical Allele Identifier: PA645485682
Gene: PEX13 HGNC NCBI

Linked Data

ClinVar Variation Id: 289819
ClinVar RCV Id: RCV000295750 RCV001140449 RCV003362747
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002609.1:p.Pro9Arg
CA10606564
NM_002618.4:c.26C>G