Canonical Allele Identifier: PA2827050660
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
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307583.1:p.Ser24Trp
CA122985
NM_001320654.2:c.71C>G