Canonical Allele Identifier: PA915957665
Gene: MYL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 639935

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000249.1:p.Ala57Val
CA73779525
NM_000258.3:c.170C>T