Canonical Allele Identifier: PA2826427139
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405084
ClinVar RCV Id: RCV000462926

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys31757Asn
CA16610218
NM_001256850.1:c.95271A>T
CA349426552
NM_001256850.1:c.95271A>C