Canonical Allele Identifier: PA2828180448
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 331990
ClinVar RCV Id: RCV000289493 RCV000381650 RCV000390435 RCV000400251 RCV000695710 RCV002392888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Lys494Asn
CA1944501
NM_001365536.1:c.1482G>T
CA349084642
NM_001365536.1:c.1482G>C