Canonical Allele Identifier: PA2826417899
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg15741Gly
CA139888
NM_001256850.1:c.47221A>G