Canonical Allele Identifier: PA2828120779
Gene: SPG7 HGNC NCBI

Linked Data

ClinVar Variation Id: 215213
ClinVar RCV Id: RCV000198775 RCV000765319 RCV001847887 RCV003993885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350779.1:p.Gly74Arg
CA323300
NM_001363850.1:c.220G>A
CA397416801
NM_001363850.1:c.220G>C