Allele Registry

Canonical Allele Identifier: PA2829848728

Gene: FCN2 HGNC NCBI

ClinVar RCV:

RCV003977273

ClinVar Variation:

3060333

HGVS (amino-acid)	Matching Registered Transcripts
NP_056652.1:p.Thr198Met	CA5321348 NM_015837.3:c.593C>T