Canonical Allele Identifier: PA179195
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166292

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Pro3303Leu
CA179191
NM_133379.5:c.9908C>T