Canonical Allele Identifier: PA915983920
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 811747
ClinVar RCV Id: RCV001002068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139281.1:p.Ser996Arg
CA406948920
NM_001145809.2:c.2986A>C
CA406948926
NM_001145809.2:c.2988C>A
CA406948927
NM_001145809.2:c.2988C>G