Canonical Allele Identifier: PA645411638
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332746
ClinVar RCV Id: RCV000272440 RCV000268248 RCV000327501 RCV000304731 RCV000538168 RCV002356452 RCV000359506 RCV003137943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val28488Ile
CA1988636
NM_001267550.2:c.85462G>A