Canonical Allele Identifier: PA915957481
Gene: CRELD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 407065
ClinVar RCV Id: RCV000458734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026887.2:p.Arg383Thr
CA2247943
NM_001031717.4:c.1148G>C