Canonical Allele Identifier: PA1139762020
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 859644
ClinVar RCV Id: RCV002505644 RCV003768971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Asp1790Asn
CA064352
NM_198056.3:c.5368G>A