Canonical Allele Identifier: PA2825872095
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 376433
ClinVar RCV Id: RCV000420899 RCV000423679 RCV000431121 RCV000438545 RCV000441378
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138387.1:p.Ile459Leu
CA16602868
NM_001144915.2:c.1375A>C
CA378321451
NM_001144915.2:c.1375A>T