Canonical Allele Identifier: PA2826100729
Gene: FGFR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1309587
ClinVar RCV Id: RCV001765756
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167536.1:p.Ser788Pro
CA370726901
NM_001174065.2:c.2362T>C