Canonical Allele Identifier: PA2827922476
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919734
ClinVar RCV Id: RCV001842718 RCV003541280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Met907Ile
CA352141527
NM_001354701.2:c.2721G>T
CA352141528
NM_001354701.2:c.2721G>C
CA352141529
NM_001354701.2:c.2721G>A