Canonical Allele Identifier: PA2826193045
Gene: PEX19 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180573.1:p.Gly262Ser
CA343256503
NM_001193644.1:c.784G>A