Canonical Allele Identifier: PA2827050762
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2576791
ClinVar RCV Id: RCV003323096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307583.1:p.Phe181Val
CA214305295
NM_001320654.2:c.541T>G