Canonical Allele Identifier: PA2829399012
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_002465.1:p.Lys1849Asn
CA394847448
NM_002474.3:c.5547G>T
CA394847449
NM_002474.3:c.5547G>C