Canonical Allele Identifier: PA139549
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46928
ClinVar RCV Id: RCV000040198 RCV000285797 RCV000310247 RCV000400546 RCV000400718 RCV000468407 RCV000346455 RCV001719767 RCV003486584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro10772Ser
CA139547
NM_133378.4:c.32314C>T