Canonical Allele Identifier: PA2827847700
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_001341297.1:p.Gly397Arg
CA357149
NM_001354368.2:c.1189G>C
CA16603309
NM_001354368.2:c.1189G>A