Allele Registry

Canonical Allele Identifier: PA111370

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV003588492

ClinVar Variation:

2735493

HGVS (amino-acid)	Matching Registered Transcripts
NP_000132.3:p.Ala362Ser	CA378327633 NM_000141.5:c.1084G>T