Canonical Allele Identifier: PA2825945689
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67997
ClinVar RCV Id: RCV000058791 RCV000620860 RCV003542283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Cys1796Ser
CA019342
NM_001160161.2:c.5387G>C
CA352140875
NM_001160161.2:c.5386T>A