Canonical Allele Identifier: PA2742029354
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2774465
ClinVar RCV Id: RCV003592348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Asp953Gly
CA352140504
NM_198056.3:c.2858A>G