Canonical Allele Identifier: PA2825393634
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1015991
ClinVar RCV Id: RCV001314929 RCV002504482 RCV004005076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Asn1883Lys
CA7921180
NM_001040113.2:c.5649T>A
CA394847083
NM_001040113.2:c.5649T>G