Allele Registry

Canonical Allele Identifier: PA2741906665

Gene: FCN2 HGNC NCBI

ClinVar RCV:

RCV003981931

ClinVar Variation:

3059902

HGVS (amino-acid)	Matching Registered Transcripts
NP_004099.2:p.Ala258Ser	CA5321361 NM_004108.3:c.772G>T