Canonical Allele Identifier: PA913195405
Gene: PEX7 HGNC NCBI

Linked Data

ClinVar Variation Id: 597078
ClinVar RCV Id: RCV000733093

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000279.1:p.Phe294Leu
CA365766786
NM_000288.4:c.880T>C
CA365766794
NM_000288.4:c.882C>A
CA365766796
NM_000288.4:c.882C>G