Canonical Allele Identifier: PA2830196022
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 501556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro14670Ser
CA1994134
NM_133378.4:c.44008C>T