Canonical Allele Identifier: PA916005660
Gene: FSCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 287052
ClinVar RCV Id: RCV000340965 RCV001001792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036550.1:p.Ala240Thr
CA8836760
NM_012418.4:c.718G>A