Canonical Allele Identifier: PA2825112508
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1735544

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly1285Asp
CA389041816
NM_000257.4:c.3854G>A