Canonical Allele Identifier: PA658815023
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 516827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn20700Asp
CA1992270
NM_001267550.2:c.62098A>G