Canonical Allele Identifier: PA645500888
Gene: SPATA16 HGNC NCBI

Linked Data

ClinVar Variation Id: 344221
ClinVar RCV Id: RCV000354596 RCV001691984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114161.3:p.Met133Val
CA2708362
NM_031955.6:c.397A>G