Canonical Allele Identifier: PA2827425247
Gene: BBS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 194995

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334973.1:p.Thr545Asn
CA241249
NM_001348044.3:c.1634C>A