Canonical Allele Identifier: PA2830195543
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala13585Ser
CA10576523
NM_133378.4:c.40753G>T