Canonical Allele Identifier: PA2825944911
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_001153633.1:p.Lys1305Asn
CA017858
NM_001160161.2:c.3915G>T
CA352147126
NM_001160161.2:c.3915G>C