Canonical Allele Identifier: PA2828180360
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 331992
ClinVar RCV Id: RCV000260488 RCV000306043 RCV000315687 RCV000356412 RCV000647753 RCV001770266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Met403Thr
CA1944567
NM_001365536.1:c.1208T>C