Canonical Allele Identifier: PA2826429014
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 516957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly33735Ala
CA1985162
NM_001256850.1:c.101204G>C