Canonical Allele Identifier: PA1139749188
Gene: SEMA4A HGNC NCBI

Linked Data

ClinVar Variation Id: 954000
ClinVar RCV Id: RCV001226377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071762.2:p.Ala5Gly
CA31028243
NM_022367.4:c.14C>G