Canonical Allele Identifier: PA891857438
Gene: MYL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 572152
ClinVar RCV Id: RCV000693467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001002841.1:p.His122Arg
CA8622728
NM_001002841.2:c.365A>G