Canonical Allele Identifier: PA112845
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 282249
ClinVar RCV Id: RCV000315486 RCV000531503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Ile119Phe
CA2918432
NM_000232.5:c.355A>T