Canonical Allele Identifier: PA1139755936
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 923410
ClinVar RCV Id: RCV001843203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Met394Leu
CA352148953
NM_198056.3:c.1180A>T
CA352148957
NM_198056.3:c.1180A>C