Canonical Allele Identifier: PA645412777
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro34864Leu
CA1985394
NM_001267550.2:c.104591C>T