Canonical Allele Identifier: PA107636
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9401
ClinVar RCV Id: RCV000010003 RCV000022946 RCV000058604 RCV000114992 RCV000183045 RCV000617238 RCV000656563 RCV002222347 RCV004532321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Asp1275Asn
CA017530
NM_198056.3:c.3823G>A