Canonical Allele Identifier: PA645412472
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 282121
ClinVar RCV Id: RCV000558599 RCV000725027 RCV001293172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Thr265Ile
CA2918275
NM_000232.5:c.794C>T