Canonical Allele Identifier: PA645410439
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332820
ClinVar RCV Id: RCV000311908 RCV000315024 RCV000368981 RCV000399596 RCV000362803 RCV000993463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp20115Asn
CA1992502
NM_001267550.2:c.60343G>A