Canonical Allele Identifier: PA184391
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179419
ClinVar RCV Id: RCV000156208 RCV000248812 RCV000713993 RCV001083518 RCV001130359 RCV001135405 RCV001135407 RCV001130360 RCV001135406 RCV003486706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp7358Tyr
CA184389
NM_001256850.1:c.22072G>T