Canonical Allele Identifier: PA2829594938
Gene: MSTN HGNC NCBI

Linked Data

ClinVar Variation Id: 3212795
ClinVar RCV Id: RCV004503715

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005250.1:p.Phe241Leu
CA2027084
NM_005259.3:c.721T>C
CA349991113
NM_005259.3:c.723C>G
CA349991114
NM_005259.3:c.723C>A