Canonical Allele Identifier: PA645416501
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 407174
ClinVar RCV Id: RCV000460985 RCV004000766
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu916Asp
CA16614155
NM_000257.4:c.2748G>T
CA389047191
NM_000257.4:c.2748G>C