Canonical Allele Identifier: PA2830230909
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Met4336Thr
CA183646
NM_133437.4:c.13007T>C