Canonical Allele Identifier: PA349576
Gene: SPG7 HGNC NCBI

Linked Data

ClinVar Variation Id: 220101
ClinVar RCV Id: RCV000205405 RCV000585273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003110.1:p.Asp650Asn
CA349575
NM_003119.4:c.1948G>A