Canonical Allele Identifier: PA916050997
Gene: BBS10 HGNC NCBI

Linked Data

ClinVar Variation Id: 704965
ClinVar RCV Id: RCV001111720 RCV000875201 RCV003948225
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078961.3:p.Ile659Leu
CA6694065
NM_024685.4:c.1975A>T
CA385808685
NM_024685.4:c.1975A>C