Allele Registry

Canonical Allele Identifier: PA2825788501

Gene: FNDC3B HGNC NCBI

ClinVar RCV:

RCV003977343

ClinVar Variation:

3060403

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128567.1:p.Thr179Ser	CA2705394 NM_001135095.2:c.536C>G CA355533160 NM_001135095.2:c.535A>T