Canonical Allele Identifier: PA2580112053
Gene: PEX7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1702473
ClinVar RCV Id: RCV002278791

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000279.1:p.Asn79Ser
CA365855821
NM_000288.4:c.236A>G