Canonical Allele Identifier: PA2830193021
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203324
ClinVar RCV Id: RCV000643054 RCV001130659 RCV001130661 RCV001130663 RCV001721184 RCV001130660 RCV001130662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala6616Thr
CA312040
NM_133378.4:c.19846G>A