ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2829442402
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
179037
ClinVar RCV Id:
RCV000155821
RCV000415349
RCV000726977
RCV001129493
RCV001129494
RCV001086291
RCV001129490
RCV001129492
RCV001129491
RCV002362823
RCV003486700
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_003310.4:p.Lys22203Thr
CA183580
NM_003319.4:c.66608A>C