Canonical Allele Identifier: PA100216
Gene: MYOC HGNC NCBI

Linked Data

ClinVar Variation Id: 2429757
ClinVar RCV Id: RCV003127210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000252.1:p.Thr438Ile
CA343723835
NM_000261.2:c.1313C>T