Canonical Allele Identifier: PA307535
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67796
ClinVar RCV Id: RCV000058570 RCV000183036 RCV002477201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Glu1138Ala
CA017144
NM_198056.3:c.3413A>C