Canonical Allele Identifier: PA141600
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47649
ClinVar RCV Id: RCV000040918 RCV000172161 RCV000542073 RCV002390173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Met32502Thr
CA141597
NM_001256850.1:c.97505T>C