Canonical Allele Identifier: PA2825449572
Gene: CRELD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3430
ClinVar RCV Id: RCV000003599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070883.2:p.Pro162Ala
CA116208
NM_001077415.3:c.484C>G