Canonical Allele Identifier: PA181566
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178153
ClinVar RCV Id: RCV000154870 RCV000157567 RCV000172603 RCV000248440 RCV000768824 RCV001082313 RCV001134948 RCV001129917 RCV001134949 RCV001134950 RCV001134951
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Glu25985Ala
CA181565
NM_133432.3:c.77954A>C