Canonical Allele Identifier: PA1139705050
Gene: MYL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 942101
ClinVar RCV Id: RCV001212017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002467.1:p.Arg156Trp
CA8622746
NM_002476.2:c.466C>T