Canonical Allele Identifier: PA2825393646
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3072312
ClinVar RCV Id: RCV004012342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Arg1891Thr
CA394846998
NM_001040113.2:c.5672G>C