Allele Registry

Canonical Allele Identifier: PA2580483251

Gene: FNDC1 HGNC NCBI

ClinVar RCV:

RCV004081208

ClinVar Variation:

2208841

HGVS (amino-acid)	Matching Registered Transcripts
NP_115921.2:p.Pro1553Ser	CA4077911 NM_032532.3:c.4657C>T