Canonical Allele Identifier: PA108333
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67844
ClinVar RCV Id: RCV000058623 RCV000183056 RCV001255563 RCV002371902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Pro1332Leu
CA017721
NM_198056.3:c.3995C>T