Canonical Allele Identifier: PA2741985655
Gene: MYH14 HGNC NCBI
ClinVar RCV:
RCV003668590
ClinVar Variation:
2799544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079005.3:p.Pro92Leu
CA9592219
NM_024729.4:c.275C>T