Allele Registry

Canonical Allele Identifier: PA302950

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000213075

RCV000547954

RCV000724101

ClinVar Variation:

196725

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243779.1:p.Val34223Ala	CA302948 NM_001256850.1:c.102668T>C