Canonical Allele Identifier: PA2830030338
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1805908
ClinVar RCV Id: RCV002470192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079005.3:p.Glu936Gln
CA9593077
NM_024729.4:c.2806G>C