Canonical Allele Identifier: PA1139735132
Gene: SCN9A HGNC NCBI
ClinVar RCV:
RCV001049718
ClinVar Variation:
846419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Asp1947dup
CA760166393
NM_001365536.1:c.5840_5842dup