Canonical Allele Identifier: PA2826192975
Gene: PEX19 HGNC NCBI

Linked Data

ClinVar Variation Id: 293227
ClinVar RCV Id: RCV000597624 RCV001084547 RCV003940089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180573.1:p.Asp166Glu
CA1197336
NM_001193644.1:c.498T>G
CA343260334
NM_001193644.1:c.498T>A