Canonical Allele Identifier: PA915977472
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 281286
ClinVar RCV Id: RCV000274468 RCV000693652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129169.1:p.Val52Gly
CA8643701
NM_001135697.3:c.155T>G