Canonical Allele Identifier: PA107693
Gene: PEX12 HGNC NCBI

Linked Data

ClinVar Variation Id: 7775
ClinVar RCV Id: RCV000008217 RCV000415755 RCV000625796 RCV002281700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000277.1:p.Ser320Phe
CA119067
NM_000286.3:c.959C>T