Canonical Allele Identifier: PA2826101221
Gene: FGFR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 223244
ClinVar RCV Id: RCV000208875
ClinVar Variation Id: 377227

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167537.1:p.Gly401Arg
CA357149
NM_001174066.2:c.1201G>C
CA16603309
NM_001174066.2:c.1201G>A