Canonical Allele Identifier: PA2825113989
Gene: MYL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073582
ClinVar RCV Id: RCV004016588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000249.1:p.Pro87Ser
CA352498049
NM_000258.3:c.259C>T