Canonical Allele Identifier: PA915993635
Gene: FGFR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 430356
ClinVar RCV Id: RCV000493180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167538.1:p.Arg706Trp
CA4718201
NM_001174067.2:c.2116C>T