Canonical Allele Identifier: PA2825112193
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3074146
ClinVar RCV Id: RCV004012688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser1065Gly
CA389045245
NM_000257.4:c.3193A>G