Canonical Allele Identifier: PA2825253953
Gene: MYL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 942101
ClinVar RCV Id: RCV001212017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001002841.1:p.Arg156Trp
CA8622746
NM_001002841.2:c.466C>T