Canonical Allele Identifier: PA2826417634
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro15279Ala
CA1994319
NM_001256850.1:c.45835C>G