Allele Registry

Canonical Allele Identifier: PA2825871697

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000417871

RCV000424365

RCV000435530

ClinVar Variation:

376162

376163

376164

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138386.1:p.Met423Ile	CA16602619 NM_001144914.1:c.1269G>T CA16602620 NM_001144914.1:c.1269G>C CA16602621 NM_001144914.1:c.1269G>A