Canonical Allele Identifier: PA2829389876
Gene: PEX19 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002848.1:p.Cys296Tyr
CA343255060
NM_002857.4:c.887G>A