Allele Registry

Canonical Allele Identifier: PA141969

Gene: TTN HGNC NCBI

ClinVar RCV:

RCV000041086

RCV000172704

RCV000560737

RCV002426582

RCV003486619

RCV004537139

ClinVar Variation:

47817

HGVS (amino-acid)	Matching Registered Transcripts
NP_597676.3:p.Pro3811Ser	CA141967 NM_133432.3:c.11431C>T