Canonical Allele Identifier: PA2830230351
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166292

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Pro3257Leu
CA179191
NM_133437.4:c.9770C>T