ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA111722
Gene: FGFR2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
13274
ClinVar RCV Id:
RCV000014194
RCV001781263
RCV001037961
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000132.3:p.Thr341Pro
CA280176
NM_000141.5:c.1021A>C