Canonical Allele Identifier: PA351914
Gene: MYL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 222736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000249.1:p.Gly128Asp
CA351912
NM_000258.3:c.383G>A