Canonical Allele Identifier: PA180849
Gene: MYL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 177841
ClinVar RCV Id: RCV000154477 RCV000201472 RCV000766488 RCV000769164 RCV000845401 RCV001309098
ClinVar Variation Id: 848489
ClinVar RCV Id: RCV001052257 RCV001089635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000249.1:p.Val156Leu
CA013890
NM_000258.3:c.466G>T
CA352495892
NM_000258.3:c.466G>C