Canonical Allele Identifier: PA2829437150
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 264208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Pro13675Ser
CA10587485
NM_003319.4:c.41023C>T