Canonical Allele Identifier: PA181454
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68024
ClinVar RCV Id: RCV000058824 RCV000154829 RCV000242689 RCV000678920 RCV001149898 RCV001149899 RCV001149900 RCV001149901 RCV001149902 RCV003149714 RCV001842403 RCV004542729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Pro2006Ala
CA019597
NM_001099404.2:c.6016C>G