Canonical Allele Identifier: PA2580177003
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2038466
ClinVar RCV Id: RCV002907628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu34797Ala
CA60956253
NM_001267550.2:c.104390A>C