Canonical Allele Identifier: PA645410021
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 281972

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg16624Gln
CA1994499
NM_001267550.2:c.49871G>A