Allele Registry

Canonical Allele Identifier: PA2829775001

Gene: NFASC HGNC NCBI

ClinVar RCV:

RCV003087593

RCV003250752

ClinVar Variation:

2160274

HGVS (amino-acid)	Matching Registered Transcripts
NP_055905.2:p.Val659Ile	CA1350151 NM_015090.4:c.1975G>A