Canonical Allele Identifier: PA2826412776
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332923
ClinVar RCV Id: RCV000275139 RCV000309232 RCV000314970 RCV000476843 RCV000366312 RCV000367396 RCV000713978 RCV000770094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro5328Leu
CA2001941
NM_001256850.1:c.15983C>T