Canonical Allele Identifier: PA2825363705
Gene: SPATA7 HGNC NCBI

Linked Data

ClinVar Variation Id: 314786
ClinVar RCV Id: RCV000300527 RCV001051680 RCV002279721 RCV001535483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035518.1:p.Ile339Thr
CA7298732
NM_001040428.4:c.1016T>C