Canonical Allele Identifier: PA2825128172
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1332221
ClinVar RCV Id: RCV001842188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Leu39Phe
CA352158790
NM_000335.5:c.117G>T
CA352158791
NM_000335.5:c.117G>C