Canonical Allele Identifier: PA112868
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 8718
ClinVar RCV Id: RCV000009256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Met100Lys
CA119858
NM_000232.5:c.299T>A