Canonical Allele Identifier: PA100041
Gene: MYOC HGNC NCBI

Linked Data

ClinVar Variation Id: 7950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000252.1:p.Ile477Ser
CA119174
NM_000261.2:c.1430T>G