Canonical Allele Identifier: PA645485908
Gene: PEX13 HGNC NCBI

Linked Data

ClinVar Variation Id: 375270
ClinVar RCV Id: RCV000416325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002609.1:p.Trp313Gly
CA16044181
NM_002618.4:c.937T>G