Canonical Allele Identifier: PA200048
Gene: SGCD HGNC NCBI
ClinVar RCV:
RCV000172778
ClinVar Variation:
192194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000328.2:p.Arg31Gly
CA200046
NM_000337.6:c.91C>G