Canonical Allele Identifier: PA200292
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 92660
ClinVar RCV Id: RCV000173087 RCV001049531 RCV001594381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Met1Val