Canonical Allele Identifier: PA2825907592
Gene: MYH14 HGNC NCBI
ClinVar RCV:
RCV003668590
ClinVar Variation:
2799544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139281.1:p.Pro92Leu
CA9592219
NM_001145809.2:c.275C>T