ClinGen Allele Registry
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Canonical Allele Identifier:
PA2829439022
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
47363
ClinVar RCV Id:
RCV000040633
RCV000172251
RCV000768917
RCV001081540
RCV002336151
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_003310.4:p.Leu16885Phe
CA140801
NM_003319.4:c.50653C>T