Canonical Allele Identifier: PA645439114
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 423721
ClinVar RCV Id: RCV000478809 RCV000984215 RCV002230956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Pro205Leu
CA8643852
NM_000023.3:c.614C>T