Canonical Allele Identifier: PA2827425971
Gene: BBS9 HGNC NCBI
ClinVar RCV:
RCV000256397
ClinVar Variation:
265988
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334975.1:p.Val140Ala
CA10588927
NM_001348046.3:c.419T>C