Canonical Allele Identifier: PA140700
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47328
ClinVar RCV Id: RCV000040598 RCV000534367 RCV000621675 RCV000724394 RCV000852812 RCV001293173 RCV003486596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn24843Asp
CA140696
NM_001267550.2:c.74527A>G