Canonical Allele Identifier: PA2827051631
Gene: BBS4 HGNC NCBI

Linked Data

ClinVar Variation Id: 412297
ClinVar RCV Id: RCV000462368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307594.1:p.Gly254Val
CA7646802
NM_001320665.2:c.761G>T