Canonical Allele Identifier: PA100239
Gene: MYOC HGNC NCBI

Linked Data

ClinVar Variation Id: 1342197
ClinVar RCV Id: RCV001838864
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000252.1:p.Trp286Arg
CA343725818
NM_000261.2:c.856T>C
CA343725820
NM_000261.2:c.856T>A