Canonical Allele Identifier: PA2828236462
Gene: RFX8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3153525
ClinVar RCV Id: RCV004438905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354438.1:p.Thr43Ser
CA347974421
NM_001367509.1:c.128C>G
CA347974424
NM_001367509.1:c.127A>T