Canonical Allele Identifier: PA209320
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 212484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro33194Leu
CA209318
NM_001267550.2:c.99581C>T