Canonical Allele Identifier: PA111664
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13272
ClinVar RCV Id: RCV000014191 RCV000014192 RCV000263144 RCV000431027 RCV000433942 RCV000440715 RCV000422979 RCV000433250 RCV000438603 RCV000552015 RCV002476961 RCV004527288 RCV004532334
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Ser252Trp
CA122985
NM_000141.5:c.755C>G