ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825872356
Gene: FGFR2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
13269
ClinVar RCV Id:
RCV000014187
RCV000014188
RCV001851846
RCV003313919
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001138388.1:p.Ala229Gly
CA280171
NM_001144916.2:c.686C>G