Allele Registry

Canonical Allele Identifier: PA256589

Gene: SCN1A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

27922

ClinVar RCV:

RCV000013743

RCV000059471

RCV000686817

RCV001253103

RCV001311218

RCV002316193

RCV004554602

ClinVar Variation:

12883

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Thr864Met	CA256587 NM_006920.6:c.2591C>T