Canonical Allele Identifier: PA302462
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191935
ClinVar RCV Id: RCV000172302 RCV000213728 RCV000233875 RCV000764323 RCV001130772 RCV001130773 RCV001130774 RCV001130775 RCV001130776 RCV001798613 RCV002433752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Met16580Val
CA302461
NM_133378.4:c.49738A>G