Canonical Allele Identifier: PA237923
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro18752Leu
CA237921
NM_001267550.2:c.56255C>T