Canonical Allele Identifier: PA2826175191
Gene: SEMA4A HGNC NCBI

Linked Data

ClinVar Variation Id: 767708
ClinVar RCV Id: RCV000946503 RCV001097416 RCV001097417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180230.1:p.Gly7Asp
CA1154880
NM_001193301.1:c.20G>A