Canonical Allele Identifier: PA916045402
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 578851
ClinVar RCV Id: RCV000701982 RCV003140111 RCV003362910
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Arg1381Gln
CA1943943
NM_001365536.1:c.4142G>A