Canonical Allele Identifier: PA2827423186
Gene: BBS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 938892
ClinVar RCV Id: RCV001208191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334970.1:p.Ala28Val
CA367189398
NM_001348041.4:c.83C>T