Canonical Allele Identifier: PA2825113024
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773897
ClinVar RCV Id: RCV003532660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1567His
CA389037824
NM_000257.4:c.4701G>T
CA389037825
NM_000257.4:c.4701G>C