ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA139316
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000040107
RCV000253899
RCV000260855
RCV000262132
RCV000300682
RCV000353220
RCV000385979
RCV000475078
RCV000725352
RCV001170630
ClinVar Variation:
46837
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_596869.4:p.Thr8918Met
CA139313
NM_133378.4:c.26753C>T