Canonical Allele Identifier: PA2826491530
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 511097
ClinVar RCV Id: RCV000601739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Met647Leu
CA349505974
NM_001267550.2:c.1939A>T
CA349505977
NM_001267550.2:c.1939A>C