Canonical Allele Identifier: PA2826420463
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala20476Thr
CA184884
NM_001256850.1:c.61426G>A