Canonical Allele Identifier: PA2829395895
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3074244
ClinVar RCV Id: RCV004012786
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002465.1:p.Val676Met
CA278638515
NM_002474.3:c.2026G>A