Canonical Allele Identifier: PA645455016
Gene: SCN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 427979
ClinVar RCV Id: RCV000498414
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004579.1:p.Ser111Leu
CA229507117
NM_004588.5:c.332C>T