Canonical Allele Identifier: PA915993498
Gene: FGFR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16286
ClinVar RCV Id: RCV000017678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167538.1:p.Asn361Ile
CA126353
NM_001174067.2:c.1082A>T