Canonical Allele Identifier: PA138785
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46621
ClinVar RCV Id: RCV000039891 RCV000118738 RCV000284293 RCV000252018 RCV000297377 RCV000336946 RCV000335998 RCV000394055 RCV000852908 RCV000770092 RCV001081837 RCV004534856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Tyr5683Cys
CA138781
NM_001267550.2:c.17048A>G