Allele Registry

Canonical Allele Identifier: PA112397

Gene: FGFR1 HGNC NCBI

ClinVar Variation Id: 16290

HGVS (amino-acid)	Matching Registered Transcripts
NP_075598.2:p.Cys381Arg	CA126356 NM_023110.3:c.1141T>C