Canonical Allele Identifier: PA1139702068
Gene: MYH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 891299
ClinVar RCV Id: RCV001126502 RCV001126503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002461.2:p.Cys906Ser
CA8392691
NM_002470.4:c.2716T>A
CA398160466
NM_002470.4:c.2717G>C