ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825061039
Gene: FGFR2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1406374
ClinVar RCV Id:
RCV001915790
RCV004538607
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000132.3:p.Leu357Ser
CA378327662
NM_000141.5:c.1070T>C