Canonical Allele Identifier: PA181111
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 177978
ClinVar RCV Id: RCV000154653 RCV000172658 RCV000251794 RCV000299433 RCV000356712 RCV000264643 RCV000298398 RCV000360237 RCV000400539 RCV001085015 RCV004534960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu18642Gln
CA181108
NM_001267550.2:c.55925T>A