Canonical Allele Identifier: PA345033
Gene: MSTN HGNC NCBI

Linked Data

ClinVar Variation Id: 65688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005250.1:p.Lys153Arg
CA345031
NM_005259.3:c.458A>G