Canonical Allele Identifier: PA178864
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166074
ClinVar RCV Id: RCV000152356 RCV000556771 RCV001719941 RCV002381478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala13635Thr
CA178861
NM_001267550.2:c.40903G>A