Canonical Allele Identifier: PA112776
Gene: FGFR1 HGNC NCBI
ClinVar RCV:
RCV000017679
ClinVar Variation:
16287
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075598.2:p.Tyr374Cys
CA126354
NM_023110.3:c.1121A>G