Canonical Allele Identifier: PA645478029
Gene: PEX12 HGNC NCBI

Linked Data

ClinVar Variation Id: 322655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000277.1:p.Ala14Asp
CA8504998
NM_000286.3:c.41C>A