Canonical Allele Identifier: PA311975
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203302
ClinVar RCV Id: RCV000312467 RCV000351045 RCV000354605 RCV000213881 RCV000391021 RCV000297374 RCV000400590 RCV000713987 RCV001079554 RCV003150081 RCV004539729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly6950Asp
CA311974
NM_001256850.1:c.20849G>A