Canonical Allele Identifier: PA913194199
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 626815
ClinVar RCV Id: RCV000770480

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1052Glu
CA389045360
NM_000257.4:c.3154A>G