Canonical Allele Identifier: PA308965
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202278
ClinVar RCV Id: RCV000184111 RCV000552070 RCV001086311 RCV004539714 RCV002415792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala744Thr
CA308962
NM_001267550.2:c.2230G>A