Canonical Allele Identifier: PA141647
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47662
ClinVar RCV Id: RCV000040931 RCV000245149 RCV000264463 RCV000263262 RCV000316083 RCV000322000 RCV000355491 RCV000361393 RCV001083917 RCV000725310 RCV001798211 RCV004534957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val34563Ala
CA141643
NM_001267550.2:c.103688T>C