Canonical Allele Identifier: PA2827922961
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2202304
ClinVar RCV Id: RCV003542446 RCV004009532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Phe1212Leu
CA352138026
NM_001354701.2:c.3636C>G
CA352138027
NM_001354701.2:c.3636C>A
CA352138032
NM_001354701.2:c.3634T>C