Allele Registry

Canonical Allele Identifier: PA178974

Gene: TTN HGNC NCBI

Linked Data

ClinVar RCV:

RCV000152399

RCV000172690

RCV000247819

RCV000261369

RCV000273970

RCV000316577

RCV000368549

RCV000369809

RCV001085387

RCV004532701

ClinVar Variation:

166164

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001254479.2:p.Gly7677Arg	CA178971 NM_001267550.2:c.23029G>A CA349516968 NM_001267550.2:c.23029G>C