Canonical Allele Identifier: PA645395474
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 376934
ClinVar RCV Id: RCV000417974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139281.1:p.Thr136Met
CA16603214
NM_001145809.2:c.407C>T