Canonical Allele Identifier: PA346472
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 180420
ClinVar RCV Id: RCV000157334 RCV000254668 RCV000466385 RCV003228908
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Lys1263del
CA346470
NM_001040113.2:c.3787_3789del
CA394860105
NM_001040113.2:c.3787A>T
CA394860112
NM_001040113.2:c.3784A>T
CA394860119
NM_001040113.2:c.3781A>T
CA394860127
NM_001040113.2:c.3778A>T