Canonical Allele Identifier: PA2827422048
Gene: BBS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 195632
ClinVar RCV Id: RCV000243461 RCV000723782 RCV001085388 RCV001165277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334967.1:p.Ser697Phe
CA242114
NM_001348038.3:c.2090C>T