Canonical Allele Identifier: PA2828180337
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 331994
ClinVar RCV Id: RCV000270280 RCV000273654 RCV000299739 RCV000368455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ile380Asn
CA1944577
NM_001365536.1:c.1139T>A