Canonical Allele Identifier: PA211826
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_000326.2:p.Ala1099Val
CA017023
NM_000335.5:c.3296C>T