Canonical Allele Identifier: PA140002
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47097
ClinVar RCV Id: RCV000040367 RCV000172661 RCV000260976 RCV000341213 RCV000316224 RCV000388261 RCV000375984 RCV001086441 RCV002433515 RCV001798161 RCV004528210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro16632Leu
CA139999
NM_001256850.1:c.49895C>T