Canonical Allele Identifier: PA2825440181
Gene: MYH14 HGNC NCBI
ClinVar RCV:
RCV000996976
ClinVar Variation:
808623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070654.1:p.Arg98His
CA309565626
NM_001077186.2:c.293G>A