Canonical Allele Identifier: PA2825393603
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3070719
ClinVar RCV Id: RCV004013229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Lys1856Asn
CA394847448
NM_001040113.2:c.5568G>T
CA394847449
NM_001040113.2:c.5568G>C