Canonical Allele Identifier: PA2826193045
Gene: PEX19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2047787
ClinVar RCV Id: RCV002918305
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Amino-acid Alleles

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