Canonical Allele Identifier: PA891861205
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 583356
ClinVar RCV Id: RCV003540851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Asn1592Tyr
CA352143646
NM_198056.3:c.4774A>T