Canonical Allele Identifier: PA1139674660
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 835759
ClinVar RCV Id: RCV001036718

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1434Pro
CA389040170
NM_000257.4:c.4301G>C