Canonical Allele Identifier: PA2825952022
Gene: NFASC HGNC NCBI
ClinVar RCV:
RCV003362413
ClinVar Variation:
2613546
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153805.1:p.Pro7Leu
CA1349365
NM_001160333.2:c.20C>T