Canonical Allele Identifier: PA645429201
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_149017.2:p.Gly277Val
CA7646802
NM_033028.5:c.830G>T