Canonical Allele Identifier: PA309601
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202563

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Met10491Thr
CA309599
NM_001267550.2:c.31472T>C