Canonical Allele Identifier: PA309054
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202312
ClinVar RCV Id: RCV000643651 RCV001721148 RCV002321739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu19619Asp
CA309052
NM_001267550.2:c.58857A>C
CA349501353
NM_001267550.2:c.58857A>T