Canonical Allele Identifier: PA2825253935
Gene: MYL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2709227
ClinVar RCV Id: RCV003592650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001002841.1:p.Ser124Phe
CA400022281
NM_001002841.2:c.371C>T