Canonical Allele Identifier: PA209319
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 212484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro30626Leu
CA209318
NM_133378.4:c.91877C>T