Canonical Allele Identifier: PA265394
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67850
ClinVar RCV Id: RCV000058629 RCV003541452 RCV003996539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Phe1343Leu
CA017772
NM_000335.5:c.4027T>C
CA352147403
NM_000335.5:c.4029C>G
CA352147404
NM_000335.5:c.4029C>A