Canonical Allele Identifier: PA309803
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202628
ClinVar RCV Id: RCV000273360 RCV000279393 RCV000315812 RCV000380458 RCV000373977 RCV000865015 RCV001721156
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg12676Pro
CA309802
NM_001256850.1:c.38027G>C