Canonical Allele Identifier: PA2829672760
Gene: RORB HGNC NCBI

Linked Data

ClinVar Variation Id: 1404933
ClinVar RCV Id: RCV001899136
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008845.2:p.Thr440Ile
CA373772634
NM_006914.4:c.1319C>T