Canonical Allele Identifier: PA110299
Gene: SEMA4A HGNC NCBI

Linked Data

ClinVar Variation Id: 3361
ClinVar RCV Id: RCV000003527 RCV000003526
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180229.1:p.Phe350Cys
CA116162
NM_001193300.1:c.1049T>G