Canonical Allele Identifier: PA181899
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178245
ClinVar RCV Id: RCV000154984 RCV001085049 RCV000730570 RCV004534979
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala5671Ser
CA181898
NM_133378.4:c.17011G>T