Canonical Allele Identifier: PA111722
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13274
ClinVar RCV Id: RCV000014194 RCV001781263 RCV001037961
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Thr341Pro
CA280176
NM_000141.5:c.1021A>C