Canonical Allele Identifier: PA311092
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala31675Thr
CA311091
NM_001256850.1:c.95023G>A