Canonical Allele Identifier: PA2828751233
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 226415
ClinVar RCV Id: RCV000211579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365174.1:p.Ser230Arg
CA10576342
NM_001378245.1:c.690T>A
CA387502913
NM_001378245.1:c.688A>C
CA387502925
NM_001378245.1:c.690T>G