Canonical Allele Identifier: PA2828441687
Gene: SEMA4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1009849
ClinVar RCV Id: RCV001307400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357496.1:p.Gly33Glu
CA342834035
NM_001370567.1:c.98G>A