Canonical Allele Identifier: PA645416628
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 407202

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1033Glu
CA16614485
NM_000257.4:c.3099T>A
CA389045618
NM_000257.4:c.3099T>G