Canonical Allele Identifier: PA2830432574
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3072317
ClinVar RCV Id: RCV004012347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Ile1670Val
CA352142778
NM_198056.3:c.5008A>G