Canonical Allele Identifier: PA183597
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179042
ClinVar RCV Id: RCV000155826 RCV000176704 RCV000336590 RCV000372440 RCV000281491 RCV000252082 RCV000284877 RCV000375751 RCV001293077 RCV001081539 RCV001170584 RCV004535001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile21910Thr
CA183594
NM_001267550.2:c.65729T>C