Canonical Allele Identifier: PA658667621
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro28946Ala
CA1988422
NM_001267550.2:c.86836C>G