Canonical Allele Identifier: PA2825495744
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3072091
ClinVar RCV Id: RCV004012121
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Met1296Leu
CA352148202
NM_001099405.2:c.3886A>T
CA352148204
NM_001099405.2:c.3886A>C