Canonical Allele Identifier: PA2580555537
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1743292
ClinVar RCV Id: RCV002337967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Val1604Ala
CA352143572
NM_198056.3:c.4811T>C