Canonical Allele Identifier: PA2826174777
Gene: SEMA4A HGNC NCBI

Linked Data

ClinVar Variation Id: 292844
ClinVar RCV Id: RCV000262251 RCV000356964 RCV001097420 RCV002519397 RCV004021360
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180229.1:p.Gly32Val
CA1154904
NM_001193300.1:c.95G>T