Canonical Allele Identifier: PA107682
Gene: PEX12 HGNC NCBI

Linked Data

ClinVar Variation Id: 92773
ClinVar RCV Id: RCV000078560 RCV000514867 RCV001082581 RCV000989844 RCV002498379 RCV004549498
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000277.1:p.Arg34Ser
CA145995
NM_000286.3:c.102A>T
CA399138866
NM_000286.3:c.102A>C