Canonical Allele Identifier: PA2825496446
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3071709
ClinVar RCV Id: RCV004016203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Glu1556Asp
CA352143762
NM_001099405.2:c.4668G>T
CA352143763
NM_001099405.2:c.4668G>C