Canonical Allele Identifier: PA311857
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203264
ClinVar RCV Id: RCV000185352 RCV000299916 RCV000305709 RCV000345779 RCV000231532 RCV000401300 RCV000395936 RCV000852906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gln5640His
CA311856
NM_001256850.1:c.16920A>T
CA349568899
NM_001256850.1:c.16920A>C