Canonical Allele Identifier: PA329832
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67684
ClinVar RCV Id: RCV000058448 RCV000455370 RCV000987223 RCV003486631 RCV003541010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala572Val
CA015275
NM_000335.5:c.1715C>T