Canonical Allele Identifier: PA645446191
Gene: MYL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 224067

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001002841.1:p.Glu11Lys
CA10575892
NM_001002841.2:c.31G>A