Canonical Allele Identifier: PA891858975
Gene: SCN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 567878
ClinVar RCV Id: RCV000688074
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004579.1:p.Glu31Asp
CA6300533
NM_004588.5:c.93G>T
CA6300534
NM_004588.5:c.93G>C