Canonical Allele Identifier: PA658814395
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 501556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro17238Ser
CA1994134
NM_001267550.2:c.51712C>T