Canonical Allele Identifier: PA645411148
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 264020
ClinVar RCV Id: RCV000243973 RCV001132451 RCV001132452 RCV001132453 RCV001132449 RCV001132450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly26368Val
CA10587474
NM_001267550.2:c.79103G>T