Canonical Allele Identifier: PA238047
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191992
ClinVar RCV Id: RCV000172361 RCV000248449 RCV000340184 RCV000282781 RCV000371985 RCV000337132 RCV000394687 RCV000603350 RCV000770054 RCV001084484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro11406Thr
CA238045
NM_001267550.2:c.34216C>A