Canonical Allele Identifier: PA2825496860
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67962
ClinVar RCV Id: RCV000058748 RCV001529380 RCV001842379 RCV004019059
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Pro1707Leu
CA018953
NM_001099405.2:c.5120C>T