Canonical Allele Identifier: PA2499230777
Gene: PEX7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1028672
ClinVar RCV Id: RCV001329779

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000279.1:p.Thr97Ser
CA365855936
NM_000288.4:c.289A>T
CA365855938
NM_000288.4:c.290C>G