Allele Registry

Canonical Allele Identifier: PA2580167641

Gene: NFASC HGNC NCBI

ClinVar RCV:

RCV003087593

RCV003250752

ClinVar Variation:

2160274

HGVS (amino-acid)	Matching Registered Transcripts
NP_001153803.1:p.Val674Ile	CA1350151 NM_001160331.2:c.2020G>A