Canonical Allele Identifier: PA311777
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203239
ClinVar RCV Id: RCV000185323 RCV000231783 RCV001170873 RCV003137753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro4571Ala
CA311776
NM_001256850.1:c.13711C>G