Canonical Allele Identifier: PA141308
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47542
ClinVar RCV Id: RCV000040811 RCV000247537 RCV000277148 RCV000298221 RCV000353169 RCV000356392 RCV000390504
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile31543Met
CA141305
NM_001267550.2:c.94629A>G