Canonical Allele Identifier: PA645412457
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 285961
ClinVar RCV Id: RCV000286709 RCV000696139 RCV000725755 RCV001148509 RCV002519200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Ile166Val
CA2918377
NM_000232.5:c.496A>G