Allele Registry

Canonical Allele Identifier: PA2826146863

Gene: PEX11B HGNC NCBI

ClinVar RCV:

RCV001877767

ClinVar Variation:

1374323

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171724.1:p.Ser154Arg	CA342121262 NM_001184795.1:c.462T>G CA342121264 NM_001184795.1:c.462T>A CA342121274 NM_001184795.1:c.460A>C