Canonical Allele Identifier: PA916045405
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 377136
ClinVar RCV Id: RCV000431693 RCV001052598 RCV004530528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Gly1393Arg
CA1943936
NM_001365536.1:c.4177G>A
CA349063285
NM_001365536.1:c.4177G>C