Canonical Allele Identifier: PA1139685920
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 892933
ClinVar RCV Id: RCV001129869 RCV002505705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139281.1:p.Arg1795His
CA9593782
NM_001145809.2:c.5384G>A