Canonical Allele Identifier: PA2829395867
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2716691
ClinVar RCV Id: RCV003513902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002465.1:p.Met665Ile
CA394868951
NM_002474.3:c.1995G>A
CA394868952
NM_002474.3:c.1995G>C
CA394868953
NM_002474.3:c.1995G>T