Canonical Allele Identifier: PA2828120746
Gene: SPG7 HGNC NCBI

Linked Data

ClinVar Variation Id: 215199
ClinVar RCV Id: RCV000389351 RCV003417714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350779.1:p.Ser30Asn
CA323832
NM_001363850.1:c.89G>A