Canonical Allele Identifier: PA112823
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 8719
ClinVar RCV Id: RCV000009257 RCV000727513
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Arg91Leu
CA119860
NM_000232.5:c.272G>T