Canonical Allele Identifier: PA2828180371
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 471080
ClinVar RCV Id: RCV000531983

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Gln425Lys
CA349085730
NM_001365536.1:c.1273C>A