ClinGen Allele Registry
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Canonical Allele Identifier:
PA2830235287
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
47291
ClinVar RCV Id:
RCV000040561
RCV000469845
RCV000764320
RCV001311960
RCV001798178
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_597681.4:p.Thr14710Lys
CA140591
NM_133437.4:c.44129C>A