Canonical Allele Identifier: PA645430132
Gene: MSTN HGNC NCBI

Linked Data

ClinVar Variation Id: 333237
ClinVar RCV Id: RCV000319193
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005250.1:p.Thr184Ile
CA2027111
NM_005259.3:c.551C>T