Canonical Allele Identifier: PA2830206582
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val22772Asp
CA310523
NM_133378.4:c.68315T>A