Canonical Allele Identifier: PA2825129152
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3074077
ClinVar RCV Id: RCV004012619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Met438Leu
CA352148400
NM_000335.5:c.1312A>T
CA352148403
NM_000335.5:c.1312A>C