This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: PA645395519
Gene: MYH14 HGNC NCBI
ClinVar RCV:
RCV000306047
ClinVar Variation:
329931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139281.1:p.Gln1198Leu
CA9593262
NM_001145809.2:c.3593A>T