Canonical Allele Identifier: PA310041
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202706
ClinVar RCV Id: RCV000268363 RCV000303761 RCV000264644 RCV000360879 RCV000299807 RCV000867223 RCV001532425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala16009Thr
CA310040
NM_001256850.1:c.48025G>A