Canonical Allele Identifier: PA129655
Gene: KEL HGNC NCBI

Linked Data

ClinVar Variation Id: 31082

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000411.1:p.Leu597Pro
CA129654
NM_000420.3:c.1790T>C