Canonical Allele Identifier: PA356166
Gene: SPG7 HGNC NCBI

Linked Data

ClinVar Variation Id: 220393
ClinVar RCV Id: RCV000206309 RCV000993072 RCV003897449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003110.1:p.Ser635Leu
CA350356
NM_003119.4:c.1904C>T