Canonical Allele Identifier: PA2825942582
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 998587
ClinVar RCV Id: RCV003770481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Met1760Ile
CA352141245
NM_001160160.2:c.5280G>A
CA352141246
NM_001160160.2:c.5280G>C
CA352141247
NM_001160160.2:c.5280G>T