Canonical Allele Identifier: PA645418192
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 407181
ClinVar RCV Id: RCV000457339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1921Gly
CA16614381
NM_000257.4:c.5761C>G