Canonical Allele Identifier: PA181902
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178246
ClinVar RCV Id: RCV000154985 RCV000172693 RCV001081624 RCV003486695 RCV004534980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile5633Thr
CA181901
NM_133378.4:c.16898T>C