Canonical Allele Identifier: PA645415192
Gene: BBS10 HGNC NCBI

Linked Data

ClinVar Variation Id: 235677
ClinVar RCV Id: RCV000224072 RCV000625184 RCV000801717 RCV000667212 RCV001706242 RCV003417800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078961.3:p.Met255Ile
CA6694290
NM_024685.4:c.765G>A
CA385814323
NM_024685.4:c.765G>T
CA385814325
NM_024685.4:c.765G>C