Canonical Allele Identifier: PA111430
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 13300
ClinVar RCV Id: RCV002513039 RCV000014227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Asp321Ala
CA280195
NM_000141.5:c.962A>C