Canonical Allele Identifier: PA2825537614
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 532122
ClinVar RCV Id: RCV003139965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Thr187Ser
CA064561
NM_001099404.2:c.560C>G
CA352153747
NM_001099404.2:c.559A>T