Canonical Allele Identifier: PA296986
Gene: MYL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 181442
ClinVar RCV Id: RCV000158945 RCV001857571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000249.1:p.Lys98Glu
CA013735
NM_000258.3:c.292A>G