Canonical Allele Identifier: PA2580112147
Gene: PEX7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1761452
ClinVar RCV Id: RCV002419036
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000279.1:p.Thr266Ser
CA365764486
NM_000288.4:c.796A>T
CA365764488
NM_000288.4:c.797C>G