Canonical Allele Identifier: PA658665654
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 448799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys15920Gln
CA1994992
NM_001267550.2:c.47758A>C