Canonical Allele Identifier: PA178449
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165751
ClinVar RCV Id: RCV000152190 RCV000246520 RCV000470539 RCV001130318 RCV001130319 RCV001130320 RCV001130321 RCV001130322 RCV003456357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu30391Asp
CA178447
NM_001267550.2:c.91173A>C
CA349503258
NM_001267550.2:c.91173A>T