Canonical Allele Identifier: PA913201374
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 626217
ClinVar RCV Id: RCV000770774 RCV001855975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139281.1:p.Glu991Lys
CA309561876
NM_001145809.2:c.2971G>A