Canonical Allele Identifier: PA211827
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67789
ClinVar RCV Id: RCV000058562 RCV000148851 RCV000183030 RCV000621290 RCV001842332 RCV002477200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ala1100Val
CA017023
NM_001099404.2:c.3299C>T