Canonical Allele Identifier: PA658665385
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467082

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro12501Leu
CA349484155
NM_001267550.2:c.37502C>T