Canonical Allele Identifier: PA658660443
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 466604
ClinVar RCV Id: RCV000544134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Thr182Pro
CA2918367
NM_000232.5:c.544A>C