Canonical Allele Identifier: PA2825493787
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 345126
ClinVar RCV Id: RCV000262047 RCV000277415 RCV000312527 RCV000315917 RCV000319498 RCV000354418 RCV000369639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Leu624Ile
CA10616342
NM_001099405.2:c.1870C>A