Canonical Allele Identifier: PA139822
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47034
ClinVar RCV Id: RCV000040304 RCV000232832 RCV000618058 RCV001132983 RCV001132985 RCV001132984 RCV001136418 RCV001136419 RCV001170659 RCV001537833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Ser1400Thr
CA139816
NM_133379.5:c.4199G>C