ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2830008741
Gene: FGFR2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
13286
ClinVar RCV Id:
RCV000014208
RCV000014209
RCV000256107
RCV000415503
RCV000528973
RCV003313920
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_075418.1:p.Ser262Cys
CA122991
NM_023029.2:c.785C>G