Canonical Allele Identifier: PA112397
Gene: FGFR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16290

Amino-acid Alleles

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