Canonical Allele Identifier: PA308947
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro17470Gln
CA308945
NM_001267550.2:c.52409C>A