Canonical Allele Identifier: PA246553
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 198061
ClinVar RCV Id: RCV000179276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000223.1:p.Met305Val
CA246551
NM_000232.5:c.913A>G