Canonical Allele Identifier: PA112694
Gene: FGFR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16300
ClinVar RCV Id: RCV000030937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075598.2:p.Pro722Ser
CA130223
NM_023110.3:c.2164C>T