Canonical Allele Identifier: PA139626
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46956
ClinVar RCV Id: RCV000040226 RCV000254284 RCV000458956 RCV000726937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Met14170Thr
CA139622
NM_001267550.2:c.42509T>C