Canonical Allele Identifier: PA2825132677
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1428511
ClinVar RCV Id: RCV003772861
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala1904Gly
CA352140224
NM_000335.5:c.5711C>G