Allele Registry

Canonical Allele Identifier: PA108287

Gene: SCN5A HGNC NCBI

Linked Data

ClinVar RCV:

RCV000041636

RCV000058821

RCV000171818

RCV000202785

RCV000251940

RCV000678922

RCV000852960

RCV001145574

RCV001145575

RCV001145687

RCV001145688

RCV001145689

RCV001841618

ClinVar Variation:

48315

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_932173.1:p.Phe2004Leu	CA019578 NM_198056.3:c.6010T>C CA065185 NM_198056.3:c.6012C>G CA352139097 NM_198056.3:c.6012C>A