Canonical Allele Identifier: PA2829594932
Gene: MSTN HGNC NCBI

Linked Data

ClinVar Variation Id: 3212788
ClinVar RCV Id: RCV004503708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005250.1:p.Met180Val
CA2027116
NM_005259.3:c.538A>G