Canonical Allele Identifier: PA141595
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47647
ClinVar RCV Id: RCV000040916 RCV000172607 RCV000246004 RCV000279530 RCV000280823 RCV000316166 RCV000375400 RCV000378875 RCV000466398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala31496Thr
CA141593
NM_133378.4:c.94486G>A