Canonical Allele Identifier: PA312099
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203343
ClinVar RCV Id: RCV000185451 RCV000643774 RCV001293081 RCV003137761 RCV004539731
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val8721Met
CA312097
NM_001267550.2:c.26161G>A