ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2829432044
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
178220
ClinVar RCV Id:
RCV000154955
RCV000252544
RCV000467649
RCV001135957
RCV001134532
RCV001135955
RCV001135956
RCV001135958
RCV001697149
RCV001798508
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_003310.4:p.Lys4593Arg
CA181823
NM_003319.4:c.13778A>G