Canonical Allele Identifier: PA645410471
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332818
ClinVar RCV Id: RCV000265408 RCV000398857 RCV000358355 RCV000306892 RCV000310552 RCV001375616 RCV003137950 RCV002460068 RCV003486817 RCV004544611 RCV000557466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu20426Phe
CA1992388
NM_001267550.2:c.61276C>T