Canonical Allele Identifier: PA2573229190
Gene: SEMA7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1687038
ClinVar RCV Id: RCV002248475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003603.1:p.Arg148Trp
CA7657257
NM_003612.5:c.442C>T