Canonical Allele Identifier: PA891845013
Gene: MYL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 585287
ClinVar RCV Id: RCV000710037
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000249.1:p.Gly161Cys
CA352495865
NM_000258.3:c.481G>T