Canonical Allele Identifier: PA220523
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 92661
ClinVar RCV Id: RCV000078412 RCV000302292 RCV000405910 RCV001085043 RCV001293238
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Tyr123Ser
CA220521
NM_000232.5:c.368A>C