Canonical Allele Identifier: PA2825441028
Gene: MYH14 HGNC NCBI
ClinVar RCV:
RCV000306047
ClinVar Variation:
329931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070654.1:p.Gln1165Leu
CA9593262
NM_001077186.2:c.3494A>T