Canonical Allele Identifier: PA2825109906
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2114780
ClinVar RCV Id: RCV003032330

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp461Gly
CA389050743
NM_000257.4:c.1382A>G