Allele Registry

Canonical Allele Identifier: PA1139748955

Gene: ADAMTS17 HGNC NCBI

ClinVar RCV:

RCV001280961

ClinVar Variation:

992507

HGVS (amino-acid)	Matching Registered Transcripts
NP_620688.2:p.Pro24Ser	CA7758771 NM_139057.4:c.70C>T