Canonical Allele Identifier: PA2825372065
Gene: BBS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 265988
ClinVar RCV Id: RCV000256397
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001028777.1:p.Val262Ala
CA10588927
NM_001033605.2:c.785T>C