Canonical Allele Identifier: PA100122
Gene: MYOC HGNC NCBI

Linked Data

ClinVar Variation Id: 1686789
ClinVar RCV Id: RCV002248294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000252.1:p.Pro481Leu
CA343723135
NM_000261.2:c.1442C>T