Canonical Allele Identifier: PA2573276154
Gene: SCN2A HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Phe1213Cys
CA349026299
NM_021007.3:c.3638T>G