ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA181688
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000154910
RCV000172226
RCV000225816
RCV000295690
RCV000299304
RCV000348240
RCV000356815
RCV000404249
RCV002345503
ClinVar Variation:
178183
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001254479.2:p.Ile28050Val
CA181685
NM_001267550.2:c.84148A>G