Canonical Allele Identifier: PA2825131166
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1735851
ClinVar RCV Id: RCV002357371 RCV004005647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Met1295Thr
CA062435
NM_000335.5:c.3884T>C