Canonical Allele Identifier: PA145913
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 92662
ClinVar RCV Id: RCV000078413 RCV000547914 RCV001288755 RCV002514376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Ser31Ile
CA145911
NM_000232.5:c.92G>T