Canonical Allele Identifier: PA2826355233
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_001239607.1:p.Gly105Val
CA7646802
NM_001252678.2:c.314G>T