Canonical Allele Identifier: PA2827422622
Gene: BBS9 HGNC NCBI
ClinVar RCV:
RCV001208191
ClinVar Variation:
938892
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334969.1:p.Ala28Val
CA367189398
NM_001348040.3:c.83C>T