Canonical Allele Identifier: PA2826410175
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178275

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala529Thr
CA182006
NM_001256850.1:c.1585G>A