Canonical Allele Identifier: PA2825221202
Gene: PC HGNC NCBI

Linked Data

ClinVar Variation Id: 305616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000911.2:p.Met1145Ile
CA6130782
NM_000920.4:c.3435G>T
CA224120529
NM_000920.4:c.3435G>A
CA381489316
NM_000920.4:c.3435G>C