ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2830213356
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
191971
ClinVar RCV Id:
RCV000172340
RCV000219175
RCV000469863
RCV000626790
RCV001131408
RCV001134387
RCV001134389
RCV001134390
RCV001134388
RCV002390415
RCV003150042
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_597676.3:p.Asp4901Asn
CA302489
NM_133432.3:c.14701G>A