ClinGen Allele Registry
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Canonical Allele Identifier:
PA107991
Gene: SCN5A
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000058462
RCV000058463
RCV000171572
RCV001842303
RCV003298119
RCV003764734
RCV004528264
ClinVar Variation:
67698
67699
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_932173.1:p.Gly639Arg
CA015554
NM_198056.3:c.1915G>A
CA015563
NM_198056.3:c.1915G>C