Canonical Allele Identifier: PA179769
Gene: BBS10 HGNC NCBI

Linked Data

ClinVar Variation Id: 166721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078961.3:p.Pro539Leu
CA179768
NM_024685.4:c.1616C>T