Allele Registry

Canonical Allele Identifier: PA2741906664

Gene: FCN2 HGNC NCBI

ClinVar RCV:

RCV003977273

ClinVar Variation:

3060333

HGVS (amino-acid)	Matching Registered Transcripts
NP_004099.2:p.Thr236Met	CA5321348 NM_004108.3:c.707C>T