Canonical Allele Identifier: PA2828502385
Gene: CRELD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3430
ClinVar RCV Id: RCV000003599

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361245.1:p.Pro162Ala
CA116208
NM_001374316.1:c.484C>G