Allele Registry

Canonical Allele Identifier: PA2829848729

Gene: FCN2 HGNC NCBI

ClinVar RCV:

RCV003981931

ClinVar Variation:

3059902

HGVS (amino-acid)	Matching Registered Transcripts
NP_056652.1:p.Ala220Ser	CA5321361 NM_015837.3:c.658G>T