Canonical Allele Identifier: PA2826417621
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly15240Ala
CA1994330
NM_001256850.1:c.45719G>C