Canonical Allele Identifier: PA2741827792
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2739064
ClinVar RCV Id: RCV003516455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Lys640Asn
CA394869168
NM_001040114.2:c.1920G>C
CA394869169
NM_001040114.2:c.1920G>T