Canonical Allele Identifier: PA2830432338
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3074553
ClinVar RCV Id: RCV004014087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Val1599Ala
CA352143603
NM_198056.3:c.4796T>C