Canonical Allele Identifier: PA178962
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166151
ClinVar RCV Id: RCV000152396 RCV000172688 RCV000246789 RCV001079307 RCV001132154 RCV001133076 RCV001132152 RCV001132153 RCV001133075 RCV002225086 RCV003486682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val8005Leu
CA178960
NM_001256850.1:c.24013G>T
CA349491420
NM_001256850.1:c.24013G>C