Canonical Allele Identifier: PA916045390
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 331965
ClinVar RCV Id: RCV000276112 RCV000340680 RCV000376885 RCV000375646 RCV000412791 RCV000647772 RCV001001973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ile1315Thr
CA1943972
NM_001365536.1:c.3944T>C