Canonical Allele Identifier: PA645410031
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332847
ClinVar RCV Id: RCV000281175 RCV000313592 RCV000336193 RCV000403902 RCV000396494 RCV003486819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile16663Thr
CA1994456
NM_001267550.2:c.49988T>C