Canonical Allele Identifier: PA2830029848
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 637025
ClinVar RCV Id: RCV000789010 RCV003317366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079005.3:p.Ile276Thr
CA9592426
NM_024729.4:c.827T>C