Allele Registry

Canonical Allele Identifier: PA181567

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000154870

RCV000157567

RCV000172603

RCV000248440

RCV000768824

RCV001082313

RCV001129917

RCV001134948

RCV001134949

RCV001134950

RCV001134951

ClinVar Variation:

178153

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_596869.4:p.Glu32357Ala	CA181565 NM_133378.4:c.97070A>C