Canonical Allele Identifier: PA2826146858
Gene: PEX11B HGNC NCBI

Linked Data

ClinVar Variation Id: 595676
ClinVar RCV Id: RCV000731296
ClinVar Variation Id: 1390576
ClinVar RCV Id: RCV001910775
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171724.1:p.Gly148Arg
CA1055618
NM_001184795.1:c.442G>A
CA342121342
NM_001184795.1:c.442G>C