Canonical Allele Identifier: PA2573275661
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1420984
ClinVar RCV Id: RCV001943689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Asn212Ser
CA349017401
NM_021007.3:c.635A>G