Canonical Allele Identifier: PA2825496213
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67895
ClinVar RCV Id: RCV000058675 RCV002223185 RCV001842364 RCV002490660 RCV004019051
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Met1469Leu
CA018283
NM_001099405.2:c.4405A>C
CA352144358
NM_001099405.2:c.4405A>T