Canonical Allele Identifier: PA211822
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67912
ClinVar RCV Id: RCV000058693 RCV000183081 RCV000148850 RCV000987201 RCV001842367 RCV001725963 RCV002336211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Val1532Ile
CA018450
NM_198056.3:c.4594G>A