Canonical Allele Identifier: PA339939
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 2095
ClinVar RCV Id: RCV000002176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035806.1:p.Met743Ile
CA339938
NM_001040716.2:c.2229G>T
CA381493411
NM_001040716.2:c.2229G>C
CA381493412
NM_001040716.2:c.2229G>A