Canonical Allele Identifier: PA2830213497
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_597676.3:p.Met5205Thr
CA309793
NM_133432.3:c.15614T>C