Canonical Allele Identifier: PA2828180356
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 538468
ClinVar RCV Id: RCV000647787 RCV001171363 RCV001311225
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Val400Met
CA349085902
NM_001365536.1:c.1198G>A