Canonical Allele Identifier: PA2827050712
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13269
ClinVar RCV Id: RCV000014187 RCV000014188 RCV001851846 RCV003313919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307583.1:p.Ala116Gly
CA280171
NM_001320654.2:c.347C>G