Allele Registry

Canonical Allele Identifier: PA2828467250

Gene: SEMA4D HGNC NCBI

ClinVar RCV:

RCV003972099

ClinVar Variation:

3055397

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358124.1:p.Ala72Thr	CA5118784 NM_001371195.1:c.214G>A