Canonical Allele Identifier: PA2825872331
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374815
ClinVar RCV Id: RCV000415483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138388.1:p.Asp221Gly
CA16043913
NM_001144916.2:c.662A>G