Canonical Allele Identifier: PA2580320216
Gene: MSTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2290349
ClinVar RCV Id: RCV004145856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005250.1:p.Gln213His
CA349991306
NM_005259.3:c.639A>T
CA349991307
NM_005259.3:c.639A>C