Canonical Allele Identifier: PA2829775001
Gene: NFASC HGNC NCBI

Linked Data

ClinVar Variation Id: 2160274
ClinVar RCV Id: RCV003087593 RCV003250752
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Amino-acid Alleles

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