Canonical Allele Identifier: PA223637
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_001180230.1:p.Met434Thr
CA223636
NM_001193301.1:c.1301T>C