Canonical Allele Identifier: PA658670696
Gene: SPG7 HGNC NCBI

Linked Data

ClinVar Variation Id: 424654
ClinVar RCV Id: RCV000515979 RCV000518245 RCV003507282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003110.1:p.Glu126Gln
CA286523796
NM_003119.4:c.376G>C