Canonical Allele Identifier: PA2825939978
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 518512
ClinVar RCV Id: RCV000617811 RCV003767770
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Glu41Asp
CA352158708
NM_001160160.2:c.123G>T
CA352158714
NM_001160160.2:c.123G>C