Canonical Allele Identifier: PA915963216
Gene: MYH14 HGNC NCBI
ClinVar RCV:
RCV000002281
ClinVar Variation:
2197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070654.1:p.Leu984Phe
CA252133
NM_001077186.2:c.2950C>T