Canonical Allele Identifier: PA178582
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165883
ClinVar RCV Id: RCV000152246 RCV000308543 RCV000311951 RCV000365300 RCV000343431 RCV000405984 RCV000724292 RCV001406798 RCV003149925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys22368Asn
CA178580
NM_001267550.2:c.67104A>C
CA349424476
NM_001267550.2:c.67104A>T