Canonical Allele Identifier: PA329762
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67625
ClinVar RCV Id: RCV000058381 RCV001664239 RCV003987344 RCV004019027
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg340Trp
CA014168
NM_000335.5:c.1018C>T