Canonical Allele Identifier: PA2825109013
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2829059
ClinVar RCV Id: RCV003749892

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly245Val
CA389052154
NM_000257.4:c.734G>T