Canonical Allele Identifier: PA915970106
Gene: CEL HGNC NCBI

Linked Data

ClinVar Variation Id: 128688
ClinVar RCV Id: RCV000116660 RCV000735342
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001798.3:p.Ala656Pro
CA231004
NM_001807.6:c.1966G>C