Canonical Allele Identifier: PA2826418629
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro17111Leu
CA237921
NM_001256850.1:c.51332C>T