Canonical Allele Identifier: PA1139704224
Gene: MSTN HGNC NCBI

Linked Data

ClinVar Variation Id: 898476
ClinVar RCV Id: RCV001142350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005250.1:p.Gln172His
CA2027119
NM_005259.3:c.516A>C
CA2027120
NM_005259.3:c.516A>T