Canonical Allele Identifier: PA131871
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42923
ClinVar RCV Id: RCV000035813 RCV004017296
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln895Glu
CA012847
NM_000257.4:c.2683C>G