Canonical Allele Identifier: PA2825112689
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2986758
ClinVar RCV Id: RCV003846413

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1422Lys
CA389040307
NM_000257.4:c.4264C>A