Canonical Allele Identifier: PA2826174803
Gene: SEMA4A HGNC NCBI
ClinVar RCV:
RCV001223689
ClinVar Variation:
951711
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180229.1:p.Ser70Gly
CA1154946
NM_001193300.1:c.208A>G