Canonical Allele Identifier: PA916051281
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_079005.3:p.Thr136Met
CA16603214
NM_024729.4:c.407C>T