Allele Registry

Canonical Allele Identifier: PA2825061198

Gene: FGFR2 HGNC NCBI

ClinVar RCV:

RCV000425939

RCV000436200

RCV000442661

ClinVar Variation:

376159

376160

376161

HGVS (amino-acid)	Matching Registered Transcripts
NP_000132.3:p.Met537Ile	CA16602616 NM_000141.5:c.1611G>T CA16602617 NM_000141.5:c.1611G>C CA16602618 NM_000141.5:c.1611G>A