Canonical Allele Identifier: PA2830194726
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_596869.4:p.Met11577Thr
CA309793
NM_133378.4:c.34730T>C