Canonical Allele Identifier: PA2826100351
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_001167536.1:p.Gly488Arg
CA357149
NM_001174065.2:c.1462G>C
CA16603309
NM_001174065.2:c.1462G>A