Canonical Allele Identifier: PA1139758829
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 978332
ClinVar RCV Id: RCV001256852 RCV003770333 RCV004004925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.His617Leu
CA72939070
NM_198056.3:c.1850A>T