Canonical Allele Identifier: PA658808793
Gene: ADAM17 HGNC NCBI

Linked Data

ClinVar Variation Id: 539948
ClinVar RCV Id: RCV000649850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003174.3:p.Ala806Pro
CA1523222
NM_003183.4:c.2416G>C