Canonical Allele Identifier: PA658672010
Gene: ADAM17 HGNC NCBI

Linked Data

ClinVar Variation Id: 472726
ClinVar RCV Id: RCV000535273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003174.3:p.Ala748Val
CA1523254
NM_003183.4:c.2243C>T