Canonical Allele Identifier: PA2828442099
Gene: SEMA4A HGNC NCBI

Linked Data

ClinVar Variation Id: 96033
ClinVar RCV Id: RCV000082098 RCV000417364 RCV001095830 RCV001095829
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357496.1:p.Met434Thr
CA223636
NM_001370567.1:c.1301T>C