Canonical Allele Identifier: PA2573088570
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 848358
ClinVar RCV Id: RCV001052099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Phe507Leu
CA352167630
NM_006514.4:c.1521C>G
CA352167631
NM_006514.4:c.1521C>A
CA352167637
NM_006514.4:c.1519T>C