ClinGen Allele Registry
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Canonical Allele Identifier:
PA147608
Gene: SCN9A
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_002968.1:p.Val991Leu
CA147606
NM_002977.3:c.2971G>T
CA357867
NM_002977.3:c.[2971G>T;2794A>C]
CA349074509
NM_002977.3:c.2971G>C