Canonical Allele Identifier: PA178889
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166094
ClinVar RCV Id: RCV000152365 RCV000458579 RCV000725663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile12474Thr
CA178887
NM_001267550.2:c.37421T>C