Canonical Allele Identifier: PA2829431794
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Met4144Thr
CA183646
NM_003319.4:c.12431T>C