Canonical Allele Identifier: PA2826414323
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46781

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr8506Met
CA139175
NM_001256850.1:c.25517C>T