Allele Registry

Canonical Allele Identifier: PA916045423

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000006733

ClinVar Variation:

6361

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Thr1475Ile	CA118155 NM_001365536.1:c.4424C>T