Canonical Allele Identifier: PA645505559
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 264236
ClinVar RCV Id: RCV000246290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Val1340Leu
CA10587574
NM_198056.3:c.4018G>C