Canonical Allele Identifier: PA2829446191
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Pro26637Leu
CA311280
NM_003319.4:c.79910C>T