Canonical Allele Identifier: PA2828441650
Gene: SEMA4A HGNC NCBI

Linked Data

ClinVar Variation Id: 954000
ClinVar RCV Id: RCV001226377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357496.1:p.Ala5Gly
CA31028243
NM_001370567.1:c.14C>G