Canonical Allele Identifier: PA138997
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46699
ClinVar RCV Id: RCV000039969 RCV001065236 RCV001130568 RCV001130567 RCV001130569 RCV001130565 RCV001130566 RCV001507605 RCV003149640 RCV004534869
ClinVar Variation Id: 46700
ClinVar RCV Id: RCV000039970
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp7145Glu
CA138994
NM_001256850.1:c.21435T>A
CA138999
NM_001256850.1:c.21435T>G