Canonical Allele Identifier: PA091232
Gene: SGCA HGNC NCBI

Linked Data

ClinVar Variation Id: 9439
ClinVar RCV Id: RCV000010046 RCV000498385 RCV000778108 RCV001194149 RCV001813972
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000014.1:p.Arg284Cys
CA120431
NM_000023.3:c.850C>T