Canonical Allele Identifier: PA181792
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96291
ClinVar RCV Id: RCV000082407 RCV000154942 RCV000298829 RCV000404084 RCV000335113 RCV000368094 RCV000299417 RCV000618716 RCV001079941 RCV001798280 RCV004542797
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val14052Ile
CA181789
NM_001256850.1:c.42154G>A