Canonical Allele Identifier: PA658665348
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro11579Ser
CA1997992
NM_001267550.2:c.34735C>T