Canonical Allele Identifier: PA2825907578
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2121815
ClinVar RCV Id: RCV003049347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139281.1:p.Arg87Thr
CA406946382
NM_001145809.2:c.260G>C