Canonical Allele Identifier: PA916045445
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 426795
ClinVar RCV Id: RCV000489681 RCV000697748 RCV002341157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Arg1631Leu
CA1943754
NM_001365536.1:c.4892G>T