Canonical Allele Identifier: PA2826417277
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro14602Thr
CA1994759
NM_001256850.1:c.43804C>A