Canonical Allele Identifier: PA645393562
Gene: SPAG17 HGNC NCBI

Linked Data

ClinVar Variation Id: 437866
ClinVar RCV Id: RCV000504571
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996879.1:p.Asp357His
CA1034400
NM_206996.4:c.1069G>C