Canonical Allele Identifier: PA1139749121
Gene: ADAMTS17 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620688.2:p.Pro574Leu
CA7758113
NM_139057.4:c.1721C>T