Canonical Allele Identifier: PA2825131063
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3070953
ClinVar RCV Id: RCV004014455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Met1244Val
CA352149242
NM_000335.5:c.3730A>G