Canonical Allele Identifier: PA915958474
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 263472
ClinVar RCV Id: RCV001190249 RCV001312487 RCV003409381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Thr674Met
CA7922457
NM_001040114.2:c.2021C>T