Canonical Allele Identifier: PA1139746828
Gene: BBS10 HGNC NCBI

Linked Data

ClinVar Variation Id: 860011
ClinVar RCV Id: RCV001066249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078961.3:p.Lys697Asn
CA385808329
NM_024685.4:c.2091A>T
CA385808330
NM_024685.4:c.2091A>C