Canonical Allele Identifier: PA2825112653
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2574110
ClinVar RCV Id: RCV003485925

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1393Pro
CA389040604
NM_000257.4:c.4178T>C