Canonical Allele Identifier: PA296998
Gene: MYL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 181448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000249.1:p.Arg94Cys
CA013710
NM_000258.3:c.280C>T