Canonical Allele Identifier: PA139863
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47051
ClinVar RCV Id: RCV000040321 RCV000242790 RCV000544938 RCV001082368 RCV000852938 RCV001798156 RCV004534904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg1453Ser
CA139860
NM_001256850.1:c.4359A>T
CA349469489
NM_001256850.1:c.4359A>C