Canonical Allele Identifier: PA645485789
Gene: PEX13 HGNC NCBI

Linked Data

ClinVar Variation Id: 336669
ClinVar RCV Id: RCV000592320 RCV001083100 RCV004549766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002609.1:p.Val286Ile
CA1673366
NM_002618.4:c.856G>A