Canonical Allele Identifier: PA645412479
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 255606
ClinVar RCV Id: RCV000244974 RCV000263039 RCV000330019 RCV000724882 RCV000815228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Gly315Arg
CA2918237
NM_000232.5:c.943G>A
CA356874926
NM_000232.5:c.943G>C