Canonical Allele Identifier: PA645413940
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 305616
ClinVar RCV Id: RCV000356215 RCV002461065 RCV003897696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035806.1:p.Met1145Ile
CA6130782
NM_001040716.2:c.3435G>T
CA224120529
NM_001040716.2:c.3435G>A
CA381489316
NM_001040716.2:c.3435G>C