Canonical Allele Identifier: PA111624
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13273
ClinVar RCV Id: RCV000014193 RCV000436870 RCV000489611 RCV000532721 RCV000762803 RCV001197223 RCV004532335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Pro253Arg
CA280174
NM_000141.5:c.758C>G