Canonical Allele Identifier: PA139308
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46832
ClinVar RCV Id: RCV000040102 RCV000143966 RCV000172683 RCV000768893 RCV000986941 RCV001081687 RCV004534882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.His9775Tyr
CA139304
NM_001256850.1:c.29323C>T