Canonical Allele Identifier: PA645410463
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro20358Leu
CA1992409
NM_001267550.2:c.61073C>T