Canonical Allele Identifier: PA2825872029
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 29855
ClinVar RCV Id: RCV000022734 RCV000493423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138387.1:p.Met302Arg
CA128693
NM_001144915.2:c.905T>G