Canonical Allele Identifier: PA915987055
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_056328.3:p.Pro162Ala
CA116208
NM_015513.6:c.484C>G