Canonical Allele Identifier: PA645414678
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 234707
ClinVar RCV Id: RCV000213114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly212Asp
CA10577514
NM_000257.4:c.635G>A