Canonical Allele Identifier: PA1139756916
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 880347
ClinVar RCV Id: RCV001108581 RCV001108583 RCV001108585 RCV001108582 RCV001108584 RCV001856447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075259.4:p.Asp522Gly
CA5720695
NM_022970.3:c.1565A>G