Allele Registry

Canonical Allele Identifier: PA2825872089

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000417871

RCV000424365

RCV000435530

ClinVar Variation:

376162

376163

376164

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138387.1:p.Met446Ile	CA16602619 NM_001144915.2:c.1338G>T CA16602620 NM_001144915.2:c.1338G>C CA16602621 NM_001144915.2:c.1338G>A