Canonical Allele Identifier: PA122997
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13295
ClinVar RCV Id: RCV000014221 RCV000014220 RCV003988821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075259.4:p.Lys527Glu
CA122996
NM_022970.3:c.1579A>G