Canonical Allele Identifier: PA111646
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 549484
ClinVar RCV Id: RCV001313539 RCV000664049 RCV003987651 RCV004527721 RCV002298724
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Ser252Leu
CA5721006
NM_000141.5:c.755C>T