Canonical Allele Identifier: PA141969
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47817
ClinVar RCV Id: RCV000041086 RCV000172704 RCV000560737 RCV003486619 RCV002426582 RCV004537139
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Pro3811Ser
CA141967
NM_133432.3:c.11431C>T