Canonical Allele Identifier: PA309795
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202625
ClinVar RCV Id: RCV000184512 RCV000318789 RCV000282780 RCV000355036 RCV000260211 RCV000322746 RCV000769024 RCV002390480
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Met14145Thr
CA309793
NM_001267550.2:c.42434T>C