Canonical Allele Identifier: PA2825392343
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2716691
ClinVar RCV Id: RCV003513902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035202.1:p.Met672Ile
CA394868951
NM_001040113.2:c.2016G>A
CA394868952
NM_001040113.2:c.2016G>C
CA394868953
NM_001040113.2:c.2016G>T