Canonical Allele Identifier: PA2741896482
Gene: MYH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2959655
ClinVar RCV Id: RCV003811830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002461.2:p.Leu899Trp
CA398160659
NM_002470.4:c.2696T>G