Canonical Allele Identifier: PA2826101067
Gene: FGFR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16286
ClinVar RCV Id: RCV000017678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167537.1:p.Asn241Ile
CA126353
NM_001174066.2:c.722A>T