Canonical Allele Identifier: PA645412401
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 283457
ClinVar RCV Id: RCV000269382 RCV001240083
ClinVar Variation Id: 420206
ClinVar RCV Id: RCV000540129 RCV000726289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Ala8_Ala9dup
CA10604499
NM_000232.5:c.18_23dup