ClinGen Allele Registry
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Canonical Allele Identifier:
PA145997
Gene: PEX12
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000078561
RCV000970690
RCV001729380
RCV002515755
RCV004549499
ClinVar Variation:
92774
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000277.1:p.Arg151Cys
CA145996
NM_000286.3:c.451C>T