ClinGen Allele Registry
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Canonical Allele Identifier:
PA118139
Gene: SCN9A
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Transcript change
NP_002968.1:p.Trp897Ter
NM_002977.3:c.2690G>A
NM_002977.3:c.2691G>A