Canonical Allele Identifier: PA178973
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166164
ClinVar RCV Id: RCV000152399 RCV000172690 RCV000316577 RCV000369809 RCV000247819 RCV000261369 RCV000273970 RCV000368549 RCV001085387 RCV004532701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly7360Arg
CA178971
NM_001256850.1:c.22078G>A
CA349516968
NM_001256850.1:c.22078G>C