Canonical Allele Identifier: PA2825495769
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67835
ClinVar RCV Id: RCV000058613 RCV000148846 RCV000470787 RCV000496069 RCV000618218 RCV000987206 RCV000824759 RCV000725469 RCV000993797 RCV001842354 RCV004537261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Thr1304Met
CA017612
NM_001099405.2:c.3911C>T