Canonical Allele Identifier: PA181453
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
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Pro2005Ala
CA019597
NM_000335.5:c.6013C>G