Canonical Allele Identifier: PA2829888716
Gene: BBS7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3015

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060660.2:p.His323Arg
CA252533
NM_018190.4:c.968A>G