Canonical Allele Identifier: PA265447
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67859
ClinVar RCV Id: RCV000058638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Lys1358Asn
CA017858
NM_000335.5:c.4074G>T
CA352147126
NM_000335.5:c.4074G>C