Canonical Allele Identifier: PA2573074979
Gene: SGCG HGNC NCBI

Linked Data

ClinVar Variation Id: 226415
ClinVar RCV Id: RCV000211579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365173.1:p.Ser248Arg
CA10576342
NM_001378244.1:c.744T>A
CA387502913
NM_001378244.1:c.742A>C
CA387502925
NM_001378244.1:c.744T>G