Canonical Allele Identifier: PA141997
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47828
ClinVar RCV Id: RCV000041097 RCV000725423 RCV000770111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile4218Thr
CA141993
NM_001267550.2:c.12653T>C