Canonical Allele Identifier: PA2825440173
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2799544
ClinVar RCV Id: RCV003668590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070654.1:p.Pro92Leu
CA9592219
NM_001077186.2:c.275C>T