Canonical Allele Identifier: PA112565
Gene: FGFR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075598.2:p.Ile300Thr
CA126355
NM_023110.3:c.899T>C