Canonical Allele Identifier: PA658805680
Gene: PEX19 HGNC NCBI

Linked Data

ClinVar Variation Id: 500756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002848.1:p.Ala85Val
CA1197428
NM_002857.4:c.254C>T