Canonical Allele Identifier: PA2827422778
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_001334969.1:p.Val262Ala
CA10588927
NM_001348040.3:c.785T>C