Canonical Allele Identifier: PA307592
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67842
ClinVar RCV Id: RCV000058621 RCV000183053 RCV000509258 RCV000589022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala1329Thr
CA017699
NM_000335.5:c.3985G>A