ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2830239871
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
229543
ClinVar RCV Id:
RCV000220841
RCV000304616
RCV000401224
RCV000301428
RCV000356180
RCV000340685
RCV000537936
RCV001171246
RCV001574925
RCV002365160
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_597681.4:p.Gly22171Val
CA1987351
NM_133437.4:c.66512G>T