Canonical Allele Identifier: PA2825538238
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2774470
ClinVar RCV Id: RCV003592352 RCV003661068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Met741Leu
CA352144506
NM_001099404.2:c.2221A>C
CA352144508
NM_001099404.2:c.2221A>T