Canonical Allele Identifier: PA2825133254
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 2178479
ClinVar RCV Id: RCV002595557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Phe38Leu
CA130594220
NM_000337.6:c.112T>C
CA362007720
NM_000337.6:c.114T>G
CA362007721
NM_000337.6:c.114T>A