Canonical Allele Identifier: PA141645
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_596869.4:p.Val31995Ala
CA141643
NM_133378.4:c.95984T>C