Canonical Allele Identifier: PA658670667
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 478046
ClinVar RCV Id: RCV000525216 RCV000762798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075259.4:p.Gly385Arg
CA378327226
NM_022970.3:c.1153G>A
CA378327227
NM_022970.3:c.1153G>C