Canonical Allele Identifier: PA2825178358
Gene: GC HGNC NCBI

Linked Data

ClinVar Variation Id: 2248060
ClinVar RCV Id: RCV004106733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000574.2:p.Thr340Ile
CA2955520
NM_000583.4:c.1019C>T