Canonical Allele Identifier: PA2828996868
Gene: SEMA3D HGNC NCBI

Linked Data

ClinVar Variation Id: 523626
ClinVar RCV Id: RCV000627055 RCV000950415 RCV003917995
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371829.1:p.His424Gln
CA4323479
NM_001384900.1:c.1272C>A
CA368025432
NM_001384900.1:c.1272C>G