Canonical Allele Identifier: PA112664
Gene: FGFR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075598.2:p.Pro366Leu
CA130222
NM_023110.3:c.1097C>T