Canonical Allele Identifier: PA181993
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178272
ClinVar RCV Id: RCV000155013 RCV000172478 RCV000464939 RCV000769134 RCV002354371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala1385Thr
CA181990
NM_133378.4:c.4153G>A