Canonical Allele Identifier: PA916045310
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 421969
ClinVar RCV Id: RCV000479461 RCV000700015 RCV001535622 RCV004023160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Arg907Trp
CA1944214
NM_001365536.1:c.2719C>T