Canonical Allele Identifier: PA913194360
Gene: MYL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 629011
ClinVar RCV Id: RCV000773697

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000249.1:p.Gly77Arg
CA352498266
NM_000258.3:c.229G>C
CA352498267
NM_000258.3:c.229G>A