Canonical Allele Identifier: PA2830202551
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg29911Ser
CA311019
NM_133378.4:c.89731C>A