Canonical Allele Identifier: PA2826425264
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196155
ClinVar RCV Id: RCV000176905 RCV002362901 RCV000228254
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu28837Asp
CA243018
NM_001256850.1:c.86511A>C
CA349501426
NM_001256850.1:c.86511A>T