Canonical Allele Identifier: PA185351
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179887
ClinVar RCV Id: RCV000156687 RCV001369508 RCV001589021 RCV002390367
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile31985Thr
CA185350
NM_133378.4:c.95954T>C