Canonical Allele Identifier: PA645409654
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405161

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro13130Leu
CA1996729
NM_001267550.2:c.39389C>T