Canonical Allele Identifier: PA2580266788
Gene: PEX19 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002848.1:p.Gly262Ser
CA343256503
NM_002857.4:c.784G>A