ClinGen Allele Registry
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Canonical Allele Identifier:
PA183589
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000155823
RCV000289428
RCV000292921
RCV000344162
RCV000352439
RCV000387336
RCV000643752
RCV001798515
RCV002354376
RCV004546441
ClinVar Variation:
179039
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001243779.1:p.Leu28356Met
CA183587
NM_001256850.1:c.85066T>A