Canonical Allele Identifier: PA2829888653
Gene: BBS7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2098931
ClinVar RCV Id: RCV003022744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060660.2:p.Lys237Asn
CA358065573
NM_018190.4:c.711G>C
CA358065574
NM_018190.4:c.711G>T