Canonical Allele Identifier: PA916045278
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 254096
ClinVar RCV Id: RCV000239913 RCV001509166 RCV002446483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Met768Ile
CA1944301
NM_001365536.1:c.2304G>A
CA349079501
NM_001365536.1:c.2304G>T
CA349079504
NM_001365536.1:c.2304G>C