Canonical Allele Identifier: PA140168
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47157
ClinVar RCV Id: RCV000040427 RCV000172654 RCV000472663 RCV000768977 RCV001132010 RCV001132952 RCV002321528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp18361Gly
CA140165
NM_001256850.1:c.55082A>G