Canonical Allele Identifier: PA645430123
Gene: MSTN HGNC NCBI

Linked Data

ClinVar Variation Id: 333242
ClinVar RCV Id: RCV000347027 RCV000762305 RCV003940339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005250.1:p.Arg88Gln
CA2027184
NM_005259.3:c.263G>A