Canonical Allele Identifier: PA645409479
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238740

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro10586Ala
CA1998862
NM_001267550.2:c.31756C>G