Canonical Allele Identifier: PA2580555446
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1971935
ClinVar RCV Id: RCV003658096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Thr1197Ser
CA352138142
NM_198056.3:c.3590C>G
CA352138144
NM_198056.3:c.3589A>T