Canonical Allele Identifier: PA916045383
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 195592
ClinVar RCV Id: RCV000176193 RCV000260317 RCV000276938 RCV000367768 RCV000487601 RCV000354077 RCV000655984 RCV001084299 RCV002362895
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Leu1278Val
CA201841
NM_001365536.1:c.3832C>G