Canonical Allele Identifier: PA2825113761
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3069690
ClinVar RCV Id: RCV004008234

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1889Gly
CA389034732
NM_000257.4:c.5666C>G