Canonical Allele Identifier: PA2825538750
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1017112
ClinVar RCV Id: RCV003541336 RCV004005084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Thr1147Ser
CA72923967
NM_001099404.2:c.3440C>G
CA352138469
NM_001099404.2:c.3439A>T