Canonical Allele Identifier: PA2825131885
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1743377
ClinVar RCV Id: RCV002330764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Leu1607Arg
CA352143150
NM_000335.5:c.4820T>G