Canonical Allele Identifier: PA2829429655
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Thr632Ala
CA10581905
NM_003319.4:c.1894A>G