Canonical Allele Identifier: PA2830242077
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47647

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ala25191Thr
CA141593
NM_133437.4:c.75571G>A