Canonical Allele Identifier: PA2826192921
Gene: PEX19 HGNC NCBI

Linked Data

ClinVar Variation Id: 500756
ClinVar RCV Id: RCV000591811 RCV001064828
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180573.1:p.Ala85Val
CA1197428
NM_001193644.1:c.254C>T