Canonical Allele Identifier: PA352157
Gene: RAPGEF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 222969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_941372.1:p.Tyr572Cys
CA352156
NM_198679.2:c.1715A>G