Canonical Allele Identifier: PA2825352635
Gene: CRELD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3429

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026887.2:p.Arg107His
CA281535
NM_001031717.4:c.320G>A