Canonical Allele Identifier: PA2826421643
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229507

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala22470Pro
CA1990515
NM_001256850.1:c.67408G>C