Canonical Allele Identifier: PA181900
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178245
ClinVar RCV Id: RCV000154984 RCV001085049 RCV000730570 RCV004534979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala6915Ser
CA181898
NM_001267550.2:c.20743G>T