Canonical Allele Identifier: PA139625
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_001243779.1:p.Met12529Thr
CA139622
NM_001256850.1:c.37586T>C