Canonical Allele Identifier: PA2828180197
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1444522
ClinVar RCV Id: RCV001982457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Leu238Phe
CA349093187
NM_001365536.1:c.714G>T
CA349093189
NM_001365536.1:c.714G>C