Canonical Allele Identifier: PA2826175000
Gene: SEMA4A HGNC NCBI

Linked Data

ClinVar Variation Id: 96033
ClinVar RCV Id: RCV000082098 RCV000417364 RCV001095830 RCV001095829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180229.1:p.Met434Thr
CA223636
NM_001193300.1:c.1301T>C