Canonical Allele Identifier: PA2829429642
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_003310.4:p.Met601Leu
CA349505974
NM_003319.4:c.1801A>T
CA349505977
NM_003319.4:c.1801A>C