Canonical Allele Identifier: PA2827422650
Gene: BBS9 HGNC NCBI
ClinVar RCV:
RCV001309012
ClinVar Variation:
1011247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334969.1:p.Leu69Pro
CA4213899
NM_001348040.3:c.206T>C