Allele Registry

Canonical Allele Identifier: PA916045383

Gene: SCN9A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

192753

ClinVar RCV:

RCV000176193

RCV000260317

RCV000276938

RCV000354077

RCV000367768

RCV000487601

RCV000655984

RCV001084299

RCV002362895

ClinVar Variation:

195592

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Leu1278Val	CA201841 NM_001365536.1:c.3832C>G