Canonical Allele Identifier: PA916045333
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 471107
ClinVar RCV Id: RCV000537875
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Met1046Ile
CA349073661
NM_001365536.1:c.3138G>T
CA349073663
NM_001365536.1:c.3138G>C
CA349073671
NM_001365536.1:c.3138G>A