Canonical Allele Identifier: PA309591
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202560
ClinVar RCV Id: RCV000313900 RCV000329199 RCV000368569 RCV000474657 RCV000273981 RCV000365255 RCV000733449 RCV004539718 RCV003387790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu10055Gln
CA309590
NM_001256850.1:c.30163G>C