Canonical Allele Identifier: PA915957666
Gene: MYL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 636485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000249.1:p.Thr64Ile
CA352498526
NM_000258.3:c.191C>T