Canonical Allele Identifier: PA141362
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47564
ClinVar RCV Id: RCV000040833 RCV000643737 RCV000725040 RCV000764305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr32047Met
CA141358
NM_001267550.2:c.96140C>T