Canonical Allele Identifier: PA658813414
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497106
ClinVar RCV Id: RCV000593381 RCV000678758 RCV001082337 RCV001662639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr9162Met
CA1999797
NM_001267550.2:c.27485C>T