Canonical Allele Identifier: PA145997
Gene: PEX12 HGNC NCBI

Linked Data

ClinVar Variation Id: 92774
ClinVar RCV Id: RCV000078561 RCV000970690 RCV001729380 RCV004549499 RCV002515755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000277.1:p.Arg151Cys
CA145996
NM_000286.3:c.451C>T